Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).

Hereditary motor and sensory neuropathy type I (HMSN I) or Charcot-Marie-Tooth (CMT) disease is an autosomal dominant peripheral neuropathy. In some CMT families linkage has been reported with either the Duffy blood group or the APOA2 gene, both located on chromosome 1q. More recently, linkage has b...

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Bibliographic Details
Main Authors:	Raeymaekers, P, Timmerman, V, De Jonghe, P, Swerts, L, Gheuens, J, Martin, J J, Muylle, L, De Winter, G, Vandenberghe, A, Van Broeckhoven, C
Format:	Artigo
Language:	Inglês
Published:	1989
Subjects:	Research Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC1683471/ https://ncbi.nlm.nih.gov/pubmed/2589322
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Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).

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