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Article Dans Une Revue Neuromuscular Disorders Année : 2003

The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene

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hal-02504320 , version 1 (10-03-2020)

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M. Chaouch, Y. Allal, A. de Sandre-Giovannoli, J.M. Vallat, A. Amer-El-Khedoud, et al.. The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene. Neuromuscular Disorders, 2003, 13 (1), pp.60-67. ⟨10.1016/S0960-8966(02)00196-7⟩. ⟨hal-02504320⟩
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