Reactome | Cirak, S

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created	[InstanceEdit:6803188] Jassal, Bijay, 2015-10-05
dbId	6803202
displayName	Cirak, S
firstname	Sebahattin
initial	S
publications	[LiteratureReference:8931643] Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of ?-dystroglycan [LiteratureReference:6803186] NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological disease [LiteratureReference:9940680] ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome
schemaClass	Person
surname	Cirak

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