Clinical and biophysical characterization of 19 GJB1 mutations-Reference-Cited by-同舟云学术

Clinical and biophysical characterization of 19 GJB1 mutations

Published:2016-09 Issue:11 Volume:3 Page:854-865
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Tsai Pei‐Chien¹²³,Yang De‐Ming⁴⁵,Liao Yi‐Chu¹²,Chiu Tai‐Yu⁴⁵,Kuo Hung‐Chou⁶,Su Yu‐Ping⁷⁸,Guo Yuh‐Cherng⁹¹⁰¹¹,Soong Bing‐Wen¹²³,Lin Kon‐Ping¹²,Liu Yo‐Tsen¹²,Lee Yi‐Chung¹²³

Affiliation:

1. Department of Neurology Taipei Veterans General Hospital Taipei 11217 Taiwan

2. Department of Neurology National Yang‐Ming University School of Medicine Taipei 11221 Taiwan

3. Brain Research Center National Yang‐Ming University Taipei 11221 Taiwan

4. Microscopy Service Laboratory Basic Research Division Department of Medical Research and Education Taipei Veterans General Hospital Taipei 11217 Taiwan

5. Institute of Biophotonics School of Medical Technology & Engineering; Biophotonics and Molecular Imaging Research Center (BMIRC) National Yang‐Ming University Taipei 11212 Taiwan

6. Department of Neurology Chang Gung Memorial Hospital at Linkou Medical Center and Chang Gung University College of Medicine Taoyuan 33302 Taiwan

7. Department of Psychiatry Cathay General Hospital Taipei 10687 Taiwan

8. School of Medicine Fu‐Jen Catholic University Taipei 24205Taiwan

9. Institute of Clinical Medicine National Yang‐Ming University Taipei 11221 Taiwan

10. Neuroscience Laboratory Department of Neurology China Medical University Hospital Taichung 40447 Taiwan

11. School of Medicine College of Medicine China Medical University Taichung 40402 Taiwan

Funder

Ministry of Science and Technology, Taiwan

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.347

Reference24 articles.

1. Genetic epidemiology of Charcot-Marie-Tooth in the general population

2. Update on Charcot–Marie–Tooth disease

3. Inherited Peripheral Neuropathies

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5. X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: Clinical and electrophysiologic study

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