Non-syndromic hearing loss caused by the dominant cis mutation R75Q with the recessive mutation V37I of the GJB2 (Connexin 26) gene
Crossref DOI link: https://doi.org/10.1038/emm.2015.32
Published Online: 2015-06-19
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Kim, Juwon
Jung, Jinsei
Lee, Min Goo
Choi, Jae Young
Lee, Kyung-A
Text and Data Mining valid from 2015-06-19
Version of Record valid from 2015-06-19
Article History
Received: 6 November 2014
Accepted: 8 March 2015
First Online: 19 June 2015
Competing interests
: The authors declare no conflict of interest.