Novel Mutations in the TMPRSS3 Gene May Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss

Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment

(2017) Xue Gao et al.   Biomed Research International

Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

(2017) Xue Gao et al.   NEURAL PLASTICITY

Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population

(2017) Jinsei Jung et al.   Scientific Reports

TMPRSS3 mutations in autosomal recessive nonsyndromic hearing loss

(2015) Saba Battelino et al.   EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY

Acquired small bowel diverticular disease: a review

(2014) DC Bosanquet et al.   BRITISH JOURNAL OF HOSPITAL MEDICINE

Proteolytic Activation of the Human Epithelial Sodium Channel by Trypsin IV and Trypsin I Involves Distinct Cleavage Sites

(2014) Silke Haerteis et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Identification of a Novel Homozygous Mutation, TMPRSS3: c.535G>A, in a Tibetan Family with Autosomal Recessive Non-Syndromic Hearing Loss

(2014) Dongyan Fan et al.   PLoS One

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

(2013) Jinwook Lee et al.   GENE

Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease

(2013) David N. Cooper et al.   HUMAN GENETICS

Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations

(2011) Nicole J. D. Weegerink et al.   JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY

Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation

(2010) Jiann-Jou Yang et al.   HUMAN GENETICS

Type II Transmembrane Serine Proteases

(2009) Thomas H. Bugge et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Genetic predisposition to human disease: allele-specific expression and low-penetrance regulatory loci

(2009) A de la Chapelle   ONCOGENE

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

(2007) Michel Guipponi   Frontiers in Bioscience-Landmark