A novel mutation of gap junction protein beta 1 gene in x-linked charcot-marie-tooth disease

Author:

Chen Sheng Dong,Li Zheng Xi,Guan Yang Tai,Zhou Xia Jun,Jiang Jian Ming,Hao Yong

Funder

National Science Foundation of China

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference19 articles.

1. Charcot-Marie-Tooth disease;Szigeti;Eur J Hum Genet,2009

2. CMT1X phenotypes represent loss of GJB1 gene function;Shy;Neurology,2007

3. Central nervous system signs in X-linked Charcot-Marie-Tooth disease after hyperventilation;Srinivasan;Pediatr Neurol,2008

4. Central motor and sensory pathway involvement in an X-linked Charcot-Marie-Tooth family;Zambelis;Acta Neurol Belg,2008

5. A V139M mutation also causes the reversible CNS phenotype in CMTX;Halbrich;Can J Neurol Sci,2008

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