Reactome | van den Elzen, C

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created	[InstanceEdit:4719368] Jassal, B, 2013-10-18
dbId	4719363
displayName	van den Elzen, C
firstname	Christa
initial	C
publications	[LiteratureReference:9940716] The expanding phenotype of POMT1 mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardation [LiteratureReference:9940798] Missense mutations in ?-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome [LiteratureReference:4719349] Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies
schemaClass	Person
surname	van den Elzen

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