Reactome | Venselaar, H

Schema > Person > Entries

created	[InstanceEdit:5607215] Garapati, P V, 2014-07-11
dbId	5607413
displayName	Venselaar, H
firstname	Hanka
initial	H
publications	[LiteratureReference:5607145] Human dectin-1 deficiency and mucocutaneous fungal infections [LiteratureReference:8955009] Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans [LiteratureReference:5678441] Dominant missense mutations in ABCC9 cause Cant� syndrome
schemaClass	Person
surname	Venselaar

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