Author:
Andreu Antonio L,Bruno Claudio,Tamburino Lucia,Gamez Josep,Shanske Sara,Cervera Carlos,Navarro Carmen,DiMauro Salvatore
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference11 articles.
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3. Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease);Tsujino;N Engl J Med,1993
4. Diagnosis of McArdle's disease by molecular genetic analysis of blood;El-Schahawi;Neurology,1996
5. McArdle's disease: a nonsense mutation in exon 1 of the muscle glycogen phosphorylase gene explains some but not all cases;Bartram;Hum Mol Genet,1993
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