A. Amraoui

KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness

Christian Kubisch, Björn C. Schroeder, Thomas Friedrich et al. · Cell · 1999 · 862 citations · Full text

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

Shin’ichiro Yasunaga, M’hamed Grati, Martine Cohen‐Salmon et al. · Nature Genetics · 1999 · 575 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

KCNQ4, a K ⁺ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway

Tatjana Kharkovets, Jean‐Pierre Hardelin, Saaïd Safieddine et al. · Proceedings of the National Academy of Sciences · 2000 · 402 citations · Full text

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Philomena Mburu, Mirna Mustapha, Anabel Varela et al. · Nature Genetics · 2003 · 338 citations

Knockout Mouse, Pdz Domain Molecule, Cause Deafness +9

Interactions in the network of Usher syndrome type 1 proteins

Avital Adato, Vincent Michel, Yoshiaki Kikkawa et al. · Human Molecular Genetics · 2004 · 239 citations

Protein Secretion, Genetics, Molecular Biology +19