Non-Syndromic Hearing Impairment in India: High Allelic Heterogeneity among Mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE

Genetic analysis of TMPRSS3 gene in the Korean population with autosomal recessive nonsyndromic hearing loss

(2013) Jinwook Lee et al.   GENE

A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect

(2013) Elham Davoudi-Dehaghani et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study

(2012) Maiko Miyagawa et al.   PLoS One

Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairment

(2011) K Lee et al.   CLINICAL GENETICS

High Frequency of the p.R34X Mutation in the TMC1 Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects

(2010) Mariem Ben Saïd et al.   Genetic Testing and Molecular Biomarkers

Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss

(2010) Jiann-Jou Yang et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations

(2009) Aslı Sırmacı et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Cochlear molecules and hereditary deafness

(2008) Denise Yan   Frontiers in Bioscience-Landmark

TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness

(2007) Michel Guipponi   Frontiers in Bioscience-Landmark