Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.

Charif, Majida

Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss. [electronic resource] - Gene Jul 2013 - 103-5 p. digital

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

1879-0038

10.1016/j.gene.2013.03.123 doi


Amino Acid Substitution
Base Sequence
Case-Control Studies
Claudins--genetics
DNA Mutational Analysis
Gene Frequency
Hearing Loss, Sensorineural--genetics
Heterozygote
Homozygote
Humans
Morocco
Mutation, Missense
Pedigree