Matches in Nanopublications for { ?s ?p "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_provenance.
- NP583083.RAq7-Sj_FzloeZpz_ijPXugrgyjZtXHKxUQBOr2_VZiR0130_assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583083.RAq7-Sj_FzloeZpz_ijPXugrgyjZtXHKxUQBOr2_VZiR0130_provenance.
- NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_provenance.
- NP479326.RA7d4oImIGHkaIpjYPDR52EXhH53fcBBIceI2SEwGGNLE130_assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP479326.RA7d4oImIGHkaIpjYPDR52EXhH53fcBBIceI2SEwGGNLE130_provenance.
- NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_provenance.
- NP496874.RA7p_4sRmz5Lk923R5xKZyODygHfAdX5Ylshexw3CDQKU130_assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496874.RA7p_4sRmz5Lk923R5xKZyODygHfAdX5Ylshexw3CDQKU130_provenance.
- NP496875.RA5sWVwMGqIuwrzmhVjG_Dg-vnMxa61ystlNmouB_b70A130_assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496875.RA5sWVwMGqIuwrzmhVjG_Dg-vnMxa61ystlNmouB_b70A130_provenance.
- assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.