Metabolic myopathies
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference77 articles.
1. Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts.
2. Assignment of Three Human Genes to Chrosomes (LDH-A to 11, TK to 17, and IDH to 20) and Evidence for Translocation between Human and Mouse Chrosomes in Somatic Cell Hybrids
3. Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin
4. Fatal infantile cytochrome c oxidase deficiency: Decrease of immunologically detectable enzyme in muscle
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4. Application of Fluorescence Difference Gel Electrophoresis Technology in Searching for Protein Biomarkers in Chick Myopia;Journal of Proteome Research;2007-10-09
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