Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.
about
Molecular screening of patients with nonsyndromic hearing loss from Nanjing city of ChinaCommon molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment.The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype.Etiology and associated GJB2 mutations in Mauritanian children with non-syndromic hearing loss.Associations between GJB2, mitochondrial 12S rRNA, SLC26A4 mutations, and hearing loss among three ethnicities.Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.
P2860
Q28703821-19E64228-DE39-4D0B-AE22-EB4A1ABEB570Q34184437-95873F13-9C4E-4E3C-A715-42601995D4D0Q34305182-AACF37E0-B53A-4591-8E20-19AE00979608Q38125413-06B1B616-5278-4EB1-9AB0-78C8D3AEA3DEQ40719129-06E2ABCB-BB15-439A-83DD-9104F0E4F810Q41232716-FC707AC0-B061-4111-A212-2FFB6A522654Q42866330-ED7B6B3F-D72F-463F-92AD-D1C7D1451EE9
P2860
Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Carrier frequencies of mutatio ...... 2) in the Moroccan population.
@en
type
label
Carrier frequencies of mutatio ...... 2) in the Moroccan population.
@en
prefLabel
Carrier frequencies of mutatio ...... 2) in the Moroccan population.
@en
P2093
P356
P1476
Carrier frequencies of mutatio ...... 2) in the Moroccan population.
@en
P2093
Abdelaziz Chafik
Abdelhamid Barakat
Halima Nahili
Hassan Rouba
Khadija Bakhouch
Lahcen Wakrim
Mohammed Hassar
Omar Abidi
Redouane Boulouiz
P304
P356
10.1089/GTE.2008.0063
P577
2008-12-01T00:00:00Z