GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico

scientific article

GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.IJPORL.2014.09.016
P698PubMed publication ID25288386

P50authorLaura E Martínez-GarzaQ57364332
P2093author name stringAngel Lugo-Trampe
José de Jesús Lugo-Trampe
Luis Daniel Campos-Acevedo
José Luis Treviño-González
Aideé Alejandra Hernández-Juárez
Israel de-la-Cruz-Ávila
P433issue12
P921main subjecthearing lossQ16035842
P304page(s)2107-2112
P577publication date2014-09-28
P1433published inInternational Journal of Pediatric OtorhinolaryngologyQ2602426
P1476titleGJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico
P478volume78

Reverse relations

cites work (P2860)
Q89750482Analyses of del(GJB6-D13S1830) and del(GJB6-D13S1834) deletions in a large cohort with hearing loss: Caveats to interpretation of molecular test results in multiplex families
Q91752172Disparities in discovery of pathogenic variants for autosomal recessive non-syndromic hearing impairment by ancestry
Q50055310Genetic basis of hearing loss in Spanish, Hispanic and Latino populations.
Q30244548Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review
Q92344367Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population
Q55189646Large scale newborn deafness genetic screening of 142,417 neonates in Wuhan, China.

Search more.