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Journal Article
Revue Neurologique, ISSN 0035-3787, 11/2008, Volume 164, Issue 11, pp. 912 - 916
Introduction: McArdle disease (glycogenosis type V) is an autosomal recessive metabolic myopathy. Defect in glycogen breakdown is due to mutations of the gene... 
Myophosphorylase | McArdle disease | PYGM | Exercise intolerance | Glycogenosis type V
Journal Article
Journal Article
Annales de Biologie Clinique, ISSN 0003-3898, 09/2007, Volume 65, Issue 5, pp. 550 - 554
Journal Article
Medicine & Science in Sports & Exercise, ISSN 0195-9131, 04/2016, Volume 48, Issue 4, pp. 673 - 679
Journal Article
Revue Neurologique, ISSN 0035-3787, 2008, Volume 164, Issue 11, pp. 912 - 916
La maladie de McArdle (glycogénose de type V) est une myopathie métabolique de transmission autosomique récessive causée par une mutation du gène de la... 
Myophosphorylase | Maladie de McArdle | McArdle disease | PYGM | Intolérance à l’effort | Glycogenosis type V | Exercise intolerance | Glycogénose de type V
Journal Article