✦ LIBER ✦

Functional analysis of connexin-32 mutants associated with X-linked dominant Charcot-Marie-Tooth disease

✍ Scribed by Hung-Li Wang; Wen-Teng Chang; Tu-Hsueh Yeh; Tony Wu; Mei-Shin Chen; Ching-Yi Wu

Book ID: 116761536
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 300 KB
Volume: 15
Category: Article
ISSN: 0969-9961
DOI: 10.1016/j.nbd.2003.11.005

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

X-linked dominant Charcot-Marie-Tooth di

X-linked dominant Charcot-Marie-Tooth disease with connexin 32 (Cx32) mutations in Koreans

✍ Y Kim; K-G Choi; KD Park; KS Lee; KW Chung; B-O Choi 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 722 KB

Connexin32 gene mutations in X-linked do

Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)

✍ E. A. M. Janssen; Stephan Kemp; Gerard W. Hensels; Ongie G. Sie; Christine E. M. 📂 Article 📅 1997 🏛 Springer 🌐 English ⚖ 31 KB

Novel mutations in the connexin 32 gene

Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth disease

✍ Charles C. Tan; Peter J. Ainsworth; Angelika F. Hahn; Patrick M. MacLeod 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 480 KB 👁 2 views

by R d G. Worton Charcot-Marie tooth disease, a pathologically and genetically heterogeneous group of disorders that causes a progressive neuropathy, is characterized by weakness and atrophy, primarily in peroneal and distal leg muscles. It is defined patholog-Mutation leads to 10s:. of this Mae 111

A family with X-linked dominant Charcot–

A family with X-linked dominant Charcot–Marie–Tooth caused by a connexin32 mutation

✍ Helene E Verhelst; Ann Lofgren; Rudy N Van Coster 📂 Article 📅 2000 🏛 Elsevier Science 🌐 English ⚖ 88 KB

MRI findings in X-linked Charcot–Marie–T

MRI findings in X-linked Charcot–Marie–Tooth disease associated with a novel connexin 32 mutation

✍ J.M. U-King-Im; E. Yiu; E.J. Donner; M. Shroff 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 714 KB

Four novel connexin 32 mutations in X–li

Four novel connexin 32 mutations in X–linked Charcot–Marie–Tooth disease with phenotypic variability

✍ G. Karadima; M. Panas; P. Floroskufi; N. Kalfakis; D. Vassilopoulos 📂 Article 📅 2005 🏛 Springer 🌐 English ⚖ 134 KB