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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Detaylı Bibliyografya
Asıl Yazarlar: Raeymaekers, P, Timmerman, V, De Jonghe, P, Swerts, L, Gheuens, J, Martin, J J, Muylle, L, De Winter, G, Vandenberghe, A, Van Broeckhoven, C
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1989
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683471/
https://ncbi.nlm.nih.gov/pubmed/2589322
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