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40. Myoadenylate deaminase deficiency with progressive muscle weakness and atrophy caused by new missense mutations in AMPD1 gene: case report in a Japanese patient. Abe M; Higuchi I; Morisaki H; Morisaki T; Osame M Neuromuscul Disord; 2000 Oct; 10(7):472-7. PubMed ID: 10996775 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]