Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)-Reference-Cited by-同舟云学术

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

Published:1997-03-17 Issue:4 Volume:99 Page:501-505
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Janssen E. A. M.,Kemp Stephan,Hensels Gerard W.,Sie Ongie G.,de Die-Smulders Christine E. M.,Hoogendijk Jessica E.,de Visser Marianne,Bolhuis Pieter A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050396.pdf

Cited by 50 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients;Neuromuscular Disorders;2016-10

2. Connexinopathies: a structural and functional glimpse;BMC Cell Biology;2016-05-24

3. Targeted Next-Generation Sequencing for Clinical Diagnosis of 561 Mendelian Diseases;PLOS ONE;2015-08-14

4. Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients;Clinical Genetics;2015-04-29

5. Hereditary Motor and Sensory Neuropathies;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

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