Research on molecular mechanisms ofMcArdle's disease (muscle glycogen phosphorylase deficiency).
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1981.tb00312.x/fullpdf
Reference17 articles.
1. [23] Muscle phosphorylase
2. Immunological studies on glycogen storage diseases type III and V. Demonstration of the presence of an immunoreactive protein in one case of muscle phosphorylase deficiency
3. Myophosphorylase deficiency: Two different molecular etiologies
4. [49a] Muscle phosphorylase b
5. Muscle protein analysis. I. High-resolution two-dimensional electrophoresis of skeletal muscle proteins for analysis of small biopsy samples.
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. McArdle's disease-muscle glycogen phosphorylase deficiency;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;1995-08
2. Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency.;Journal of Clinical Investigation;1993-10-01
3. Rhabdomyolysis in Childhood: A Primer on Normal Muscle Function and Selected Metabolic Myopathies Characterized by Disordered Energy Production;Pediatric Clinics of North America;1992-08
4. Histochemical and Biochemical Studies in a Patient with Myophosphorylase Deficiency;European Neurology;1990
5. McArdle's disease: Biochemical and molecular genetic studies;Annals of Neurology;1988-12
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