Reactome | Berger, EG

Schema > Person > Entries

created	[InstanceEdit:4717398] Jassal, B, 2013-10-17
dbId	4717385
displayName	Berger, EG
firstname	E G
initial	EG
publications	[LiteratureReference:4724286] Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic [LiteratureReference:4717390] Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie [LiteratureReference:4717386] MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If
schemaClass	Person
surname	Berger

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