EPS8, encoding an actin-binding protein of cochlear hair...

Orphanet Journal of Rare Diseases 2014 / 12 Vol. 9; Iss. 1

EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness

Behlouli, Asma, Bonnet, Crystel, Abdi, Samia, Bouaita, Aïcha, Lelli, Andrea, Hardelin, Jean-Pierre, Schietroma, Cataldo, Rous, Yahia, Louha, Malek, Cheknane, Ahmed, Lebdi, Hayet, Boudjelida, Kamel, Ma
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Volume:
9
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/1750-1172-9-55
Date:
December, 2014
File:
PDF, 1.14 MB
english, 2014
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