Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness

Objective: To assess the contribution of the dHMN-VII predisposition gene to peroneal muscular atrophy syndromes associated with vocal cord weakness. Methods: Linkage analysis of microsatellite markers at chromosome 2q14 was undertaken on two families, one affected by HMSN-IIC and a second manifesti...

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Detaylı Bibliyografya
Asıl Yazarlar: McEntagart, M, Dunstan, M, Bell, C, Boltshauser, E, Donaghy, M, Harper, P, Williams, N, Teare, M, Rahman, N
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Group 2002
Konular:
Short Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1757353/
https://ncbi.nlm.nih.gov/pubmed/12438487
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.73.6.762
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