A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.

Charcot-Marie-Tooth disease (CMT) is a heterogeneous group of disorders that affect the peripheral nervous system. Three loci are known for the autosomal dominant forms of axonal CMT (CMT2), but none have yet been identified for autosomal recessive axonal CMT (ARCMT2). We have studied a large consan...

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Main Authors: Bouhouche, A, Benomar, A, Birouk, N, Mularoni, A, Meggouh, F, Tassin, J, Grid, D, Vandenberghe, A, Yahyaoui, M, Chkili, T, Brice, A, LeGuern, E
Formato: Artigo
Idioma:Inglês
Publicado: 1999
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377978/
https://ncbi.nlm.nih.gov/pubmed/10441578
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