At the speed of sound: gene discovery in the auditory system
about
An acoustic gap between the NICU and womb: a potential risk for compromised neuroplasticity of the auditory system in preterm infantsExtracellular gentamicin reduces the activity of connexin hemichannels and interferes with purinergic Ca(2+) signaling in HeLa cells.Diagnostic application of targeted resequencing for familial nonsyndromic hearing loss.Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel. ACMG statementDFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12.Mutations of TMC1 cause deafness by disrupting mechanoelectrical transductionNon-syndromic autosomal-dominant deafness.Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population.Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64Genetic mutations in non-syndromic deafness patients of Uyghur and Han Chinese ethnicities in Xinjiang, China: a comparative studyGenetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing loss.Expression of deafness protein Tmie in postnatal developmental stages of C57BL/6J mice.Identification of candidate regions for a novel Usher syndrome type II locus.Attitudes of the broader hearing, deaf, and hard-of-hearing community toward genetic testing for deafness.Mechanism of two novel human GJC3 missense mutations in causing non-syndromic hearing loss.Causes of hearing impairment in the Norwegian paediatric cochlear implant program.Genetic testing as part of the early hearing detection and intervention (EHDI) process.Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations.Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis.Deaf Community and Genetics
P2860
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P2860
At the speed of sound: gene discovery in the auditory system
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
At the speed of sound: gene discovery in the auditory system
@ast
At the speed of sound: gene discovery in the auditory system
@en
type
label
At the speed of sound: gene discovery in the auditory system
@ast
At the speed of sound: gene discovery in the auditory system
@en
prefLabel
At the speed of sound: gene discovery in the auditory system
@ast
At the speed of sound: gene discovery in the auditory system
@en
P2093
P2860
P356
P1476
At the speed of sound: gene discovery in the auditory system
@en
P2093
Resendes BL
Williamson RE
P2860
P304
P356
10.1086/324122
P407
P577
2001-09-27T00:00:00Z