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

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

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Chaouch, M. | Allal, Y. | de Sandre-Giovannoli, A. | Vallat, J.M. | Amer-El-Khedoud, A. | Kassouri, N. | Chaouch, A. | Sindou, P. | Hammadouche, T. | Tazir, M. | Lévy, N. | Grid, D.

Edité par CCSD ; Elsevier -

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Langue: en

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