SMN gene analysis of the spinal form of Charcot-Marie-Tooth disease.

The spinal form of Charcot-Marie-Tooth disease (spinal CMT) is a rare genetic disorder of the peripheral nervous system, the genetic basis of which remains unknown. To test the hypothesis that a defect of survival motor neuron (SMN), the determining gene for spinal muscular atrophy (SMA), would resu...

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Detalhes bibliográficos
Main Authors: Hanash, A, Leguern, E, Birouk, N, Clermont, O, Pouget, J, Bouche, P, Munnich, A, Brice, A, Melki, J
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050977/
https://ncbi.nlm.nih.gov/pubmed/9192274
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