Results 121 to 128 of about 244,526 (128)

Cochlear pathology of the circling mouse: a new mouse model of DFNB6

Acta Oto-Laryngologica, 2007
Sung Hwa Hong, Zae Young Ryoo, Won Ho Chung   +2 more
exaly  

Localization of a Novel Autosomal Recessive Non-syndromic Hearing Impairment Locus DFNB63 to Chromosome 11q13.3-q13.4

Annals of Human Genetics, 2007
exaly  

Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53

Molecular Genetics and Genomics, 2015
Mhamed Grati, Duygu Duman, Masmoudi Saber   +2 more
exaly  

A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60

Human Genetics, 2016
Mhamed Grati, Yukio Kato, Noritaka Nakamichi   +2 more
exaly  

Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations

Iranian Journal of Public Health
Somayeh Reiisi, Fatemeh Azadegan, Mahboobeh Koohiyan   +2 more
exaly  

The pathogenic roles of the p.R130S prestin variant in DFNB61 hearing loss

Journal of Physiology
Kazuaki Homma
exaly  

A Novel Recurrent 200 kb CRYL1 Deletion Underlies DFNB1A Hearing Loss in Patients from Northwestern Spain

Genes
Juan Cadiñanos, Raquel Capin, Guadalupe Alvarez Cifuentes   +2 more
exaly  

Genotype–phenotype analysis of hearing function in patients with DFNB1A caused by the c.-23+1G>A splice site variant of the GJB2 gene (Cx26)

PLoS ONE
Nikolay A Barashkov
exaly