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14. A new rare mutation (691delCC/insAAA) in exon 17 of the PYGM gene causing McArdle disease. Quintans B; Sanchez-Andrade A; Teijeira S; Fernandez-Hojas R; Rivas E; López MJ; Navarro C Arch Neurol; 2004 Jul; 61(7):1108-10. PubMed ID: 15262743 [TBL] [Abstract][Full Text] [Related]
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16. Do carriers of PYGM mutations have symptoms of McArdle disease? Andersen ST; Dunø M; Schwartz M; Vissing J Neurology; 2006 Aug; 67(4):716-8. PubMed ID: 16924035 [TBL] [Abstract][Full Text] [Related]
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20. Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology. Ortuño-Costela MDC; Cerrada V; Moreno-Izquierdo A; García-Consuegra I; Laberthonnière C; Delourme M; Garesse R; Arenas J; Fuster García C; García García G; Millán JM; Magdinier F; Gallardo ME Int J Mol Sci; 2022 Nov; 23(22):. PubMed ID: 36430443 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]