Robert A Hegele. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh: See more » CodonDNA/geneticsGenotypeHumansLamin Type A/geneticsLipodystrophy/geneticsMetabolic Diseases/geneticsPhenotype
Substances: See more » CodonLamin Type Alamin CDNA
Year: 2007 PMID: 18056782 DOI: 10.1210/jc.2007-2078
Source DB: PubMed Journal: J Clin Endocrinol Metab ISSN: 0021-972X Impact factor: 5.958