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Matches in Nanopublications for { ?s ?p "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP257218.RAl5Z0UGHZjiJh0KWkbELs3IyPrRih3bczqmXtKIoFT-Y130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257218.RAl5Z0UGHZjiJh0KWkbELs3IyPrRih3bczqmXtKIoFT-Y130_provenance.
• NP549082.RA-eg5jU8-27ujv3UQbt7r0l1ubHJuUtoqYgYWjiF23IQ130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549082.RA-eg5jU8-27ujv3UQbt7r0l1ubHJuUtoqYgYWjiF23IQ130_provenance.
• NP625571.RAGkmlP7Iv-wuTlG_6LSvOGw0CkThmYawfc-gnw0VyXGE130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625571.RAGkmlP7Iv-wuTlG_6LSvOGw0CkThmYawfc-gnw0VyXGE130_provenance.
• NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_provenance.
• NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_provenance.
• NP829040.RAE9yWZjODfO66x7chBOuk8Hc51Q440WjPH_WcpCOB-gs130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829040.RAE9yWZjODfO66x7chBOuk8Hc51Q440WjPH_WcpCOB-gs130_provenance.
• NP915705.RAVHyoYIB5Khzkyks2b7oAGIbOLhqspkA0oIsO5LdFxP4130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915705.RAVHyoYIB5Khzkyks2b7oAGIbOLhqspkA0oIsO5LdFxP4130_provenance.
• NP915714.RAbubnwd40FRv1dtIDnEJwvIzlH40CXy-F-jPkco7gEUc130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915714.RAbubnwd40FRv1dtIDnEJwvIzlH40CXy-F-jPkco7gEUc130_provenance.
• NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_provenance.
• NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915729.RAxCnxmEpwebq6iK6AJOPur22DCmkm8WfngSstmRnq8nw130_provenance.
• NP1041595.RAYmoF2a9tSVff6QdIdSb8XA6a36VDXoPyR2gxyeAfmxU130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1041595.RAYmoF2a9tSVff6QdIdSb8XA6a36VDXoPyR2gxyeAfmxU130_provenance.
• assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1041594.RALddfz5x7H4ijZwuvBTRCIdTlZFejUCLZnDaF6R-UXWo130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1041594.RALddfz5x7H4ijZwuvBTRCIdTlZFejUCLZnDaF6R-UXWo130_provenance.
• NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_provenance.