| Literature DB >> 15979037 |
Paul J Isackson1, Mark Tarnopolsky, Georgirene D Vladutiu.
Abstract
A Caucasian family appeared to transmit McArdle disease in an autosomal dominant manner and was examined for mutations in the myophosphorylase gene. The asymptomatic father was heterozygous for the R49X mutation in exon 1. The symptomatic mother was a compound heterozygote for R49X and a novel 2 bp deletion in exon 1 causing a frameshift at codon 25 (T25fs). Each of three children manifested symptoms of McArdle disease and was either a compound heterozygote for these two mutations or homozygous for R49X.Entities:
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Year: 2005 PMID: 15979037 DOI: 10.1016/j.ymgme.2005.03.002
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797