Reactome | Gissen, P

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created	[InstanceEdit:5628739] Jassal, Bijay, 2014-10-23
dbId	5628811
displayName	Gissen, P
firstname	Paul
initial	P
publications	[LiteratureReference:5660730] The monoamine neurotransmitter disorders: an expanding range of neurological syndromes [LiteratureReference:5660723] Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia [LiteratureReference:5660704] Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study [LiteratureReference:5628748] Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease
schemaClass	Person
surname	Gissen

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