The molecular genetic basis of myophosphorylase deficiency (McArdle's disease)
Author:
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Reference36 articles.
1. McArdle's disease: a nonsense mutation in exon 1 of the muscle glycogen phosphorylase gene explains some but not all cases
2. Evidence to implicate translation by ribosomes in the mechanism by which nonsense codons reduce the nuclear level of human triosephosphate isomerase mRNA.
3. Intron/exon structure of the human gene for the muscle isozyme of glycogen phosphorylase
4. Dominant Inheritance of McArdle Syndrome
5. Congenital myopathy due to phosphorylase deficiency
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