[Genetic aspects of primary myopathies, infantile progressive spinal atrophy (Werdnig-Hoffman atrophy) and neural atrophy (Charcot-Marie-Tooth disease)].
D001284:Atrophy; D002607:Charcot-Marie-Tooth Disease; D005823:Genetics; D006801:Humans; D009134:Muscular Atrophy, Spinal; D009135:Muscular Diseases; D011502:Protein-Energy Malnutrition
GENETICS; PROGRESSIVE MUSCULAR ATROPHY
Aspects génétiques des myopathies primitives, de l'atrophie spinale progressive infantile (Werdnig-Hoffmann) et de l'atrophie neurale (Charcot-Marie-Tooth).