Matches in Nanopublications for { ?s ?p "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP210647.RAh92C396ydlw3XwLnwkNX8_2hyuKGnyVz7lycJohWnRI130_assertion description "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210647.RAh92C396ydlw3XwLnwkNX8_2hyuKGnyVz7lycJohWnRI130_provenance.
- NP590211.RAt0DhcyyBtkGMQ0jgi5_tsMg9C2suoWvp_rRkpqxMF98130_assertion description "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP590211.RAt0DhcyyBtkGMQ0jgi5_tsMg9C2suoWvp_rRkpqxMF98130_provenance.
- NP398751.RA6qgrvUReEqP4ZwlYgQsmFP6qIG3fG0CNrra7KLmGaVg130_assertion description "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP398751.RA6qgrvUReEqP4ZwlYgQsmFP6qIG3fG0CNrra7KLmGaVg130_provenance.
- NP461155.RACSd6-v4t6nQQIC5N6y5KoAP2aHWTpaLv_dd4v50sKP8130_assertion description "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461155.RACSd6-v4t6nQQIC5N6y5KoAP2aHWTpaLv_dd4v50sKP8130_provenance.
- NP831523.RA-Z4FCCSlYl76pz3JUy8elbSd9_6HuhfH05ZTZ-LRfGA130_assertion description "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831523.RA-Z4FCCSlYl76pz3JUy8elbSd9_6HuhfH05ZTZ-LRfGA130_provenance.
- NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_assertion description "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_provenance.
- NP831609.RAPMk26G2Z8sxY0YLTU2eAxFiw1oig1arQRfkg3hUJnXo130_assertion description "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831609.RAPMk26G2Z8sxY0YLTU2eAxFiw1oig1arQRfkg3hUJnXo130_provenance.
- NP461158.RAHLWYr4bTPCJbFzPJ2fdEfpEOqHmO5Vh2QNHF91DboHU130_assertion description "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461158.RAHLWYr4bTPCJbFzPJ2fdEfpEOqHmO5Vh2QNHF91DboHU130_provenance.
- NP831452.RArrXgOnD8LZyRFPG-CRpHV-yRnD3TkEymbI0dazor9JM130_assertion description "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831452.RArrXgOnD8LZyRFPG-CRpHV-yRnD3TkEymbI0dazor9JM130_provenance.