| Literature DB >> 15172004 |
Alexander B Kenton1, Ximena Sanchez, Karen J Coveler, Kimberly A Makar, Shinawe Jimenez, Fukiko Ichida, Ross T Murphy, Perry M Elliott, William McKenna, Neil E Bowles, Jeffrey A Towbin, Karla R Bowles.
Abstract
Isolated left ventricular noncompaction (LVNC) is a form of cardiomyopathy that most commonly presents in infancy with a hypertrophic and dilated left ventricle characterized by deep trabeculations and intertrabecular recesses. Our goal was to determine the frequency of mutations in G4.5, alpha-dystrobrevin, and FK Binding protein-12 in isolated LVNC patients. No mutations were identified in 47 of the 48 patients studied, while a splice site acceptor site mutation of intron 10 of G4.5 was identified in one patient, resulting in the deletion of exon 10 from the mRNA.Entities:
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Year: 2004 PMID: 15172004 DOI: 10.1016/j.ymgme.2004.02.009
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797