DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss

Autosomal Dominant Progressive Sensorineural Hearing Loss Due to a Novel Mutation in the KCNQ4 Gene

(2011) Jameson Arnett et al.   ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY

Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation

(2010) A. Xia et al.   Disease Models & Mechanisms

Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing

(2010) A. E. Shearer et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Mutation in theCOCHgene is associated with superior semicircular canal dehiscence

(2009) Michael S. Hildebrand et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment

(2009) Matías Morín et al.   HUMAN MOLECULAR GENETICS

A Contemporary Review of AudioGene audioprofiling: A machine-based candidate gene prediction tool for autosomal dominant nonsyndromic hearing loss

(2009) Michael S. Hildebrand et al.   LARYNGOSCOPE

Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss

(2009) Ángeles Mencía et al.   NATURE GENETICS

Histopathology of Nonsyndromic Autosomal Dominant Midfrequency Sensorineural Hearing Loss

(2009) Fayez Bahmad et al.   OTOLOGY & NEUROTOLOGY

Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation inWFS1

(2008) Michael S. Hildebrand et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer

(2008) Rob W J Collin et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus

(2008) Michael S Hildebrand et al.   GENETICS IN MEDICINE

Characterization of a Spontaneous, Recessive, Missense Mutation Arising in the Tecta Gene

(2008) Miguel Ángel Moreno-Pelayo et al.   JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY

A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families

(2007) Fatemeh Alasti et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY