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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Bibliografski detalji
Glavni autori: 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
Jezik:Inglês
Izdano: 1989
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683471/
https://ncbi.nlm.nih.gov/pubmed/2589322
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