W L Nyhan. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh: See more » Athetosis/geneticsAutistic Disorder/etiologyChildChild Behavior Disorders/etiologyChild, PreschoolDe Lange Syndrome/complicationsErythrocytes/enzymologyGlucosephosphate Dehydrogenase Deficiency/complicationsHumansIntellectual Disability/geneticsLesch-Nyhan Syndrome/geneticsMalePedigreePentosyltransferases/metabolismPurine-Pyrimidine Metabolism, Inborn Errors/geneticsSelf Mutilation/geneticsSex Chromosome Aberrations/complications
Substances: See more » Pentosyltransferases
Year: 1972 PMID: 5046967 DOI: 10.1203/00006450-197201000-00001
Source DB: PubMed Journal: Pediatr Res ISSN: 0031-3998 Impact factor: 3.756