T M Schroeder. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » ChildChromatidsChromosome AberrationsFanconi Syndrome/enzymologyFanconi Syndrome/geneticsHexokinase/metabolismHumansMale
Substances: See more » Hexokinase
Year: 1966 PMID: 5986057 DOI: 10.1007/bf00273021
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348