GJB1 c.196G>C ;(p.D66H)

Variant ID: X-70443753-G-C

NM_000166.5(GJB1):c.196G>C;(p.D66H)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1).

Neurology
Panosyan, Francis B FB; Laura, Matilde M; Rossor, Alexander M AM; Pisciotta, Chiara C; Piscosquito, Giuseppe G; Burns, Joshua J; Li, Jun J; Yum, Sabrina W SW; Lewis, Richard A RA; Day, John J; Horvath, Rita R; Herrmann, David N DN; Shy, Michael E ME; Pareyson, Davide D; Reilly, Mary M MM; Scherer, Steven S SS; ,
Publication Date: 2017-08-29

Variant appearance in text: GJB1: Asp66His
PubMed Link: 28768847
Variant Present in the following documents:
  • Main text
  • NEUROLOGY2017803221.pdf
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Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.

Brain Research
Hoang Dinh, Emilie E; Ahmad, Shoeb S; Chang, Qing Q; Tang, Wenxue W; Stong, Benjamin B; Lin, Xi X
Publication Date: 2009-06-24

Variant appearance in text: GJB1: D66H
PubMed Link: 19230829
Variant Present in the following documents:
  • Main text
View BVdb publication page