E Meyer, T Eggermann, H A Wollmann. Show Affiliations »
Abstract
Entities: Disease Gene Species
Mesh: See more » Abnormalities, Multiple/geneticsBone and Bones/abnormalitiesCase-Control StudiesCraniofacial Abnormalities/geneticsDwarfism/geneticsFetal Growth Retardation/geneticsGenetic VariationGermanyHumansMembrane Proteins/geneticsPolymorphism, GeneticPotassium Channels, Voltage-Gated/geneticsReference ValuesSyndrome
Substances: See more » KCNQ1OT1 protein, humanMembrane ProteinsPotassium Channels, Voltage-Gated
Year: 2005 PMID: 15781202 DOI: 10.1016/j.ymgme.2004.12.002
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797