High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals.

Wattanasirichaigoon, D

High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals. [electronic resource] - Clinical genetics Nov 2004 - 452-60 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0009-9163

10.1111/j.1399-0004.2004.00325.x doi


Adolescent
Amino Acid Substitution--genetics
Asian People--genetics
Child
Child, Preschool
Connexin 26
Connexins--genetics
Female
Hearing Loss, Sensorineural--ethnology
Humans
Infant
Isoleucine--genetics
Male
Mutation, Missense--genetics
Prevalence
Thailand
Valine--genetics