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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 , Dominique Weil , Aziz El-Amraoui , et al.
Nature Genetics, 2003, 34, pp.421-428. ⟨10.1038/ng1208⟩
Journal articles pasteur-03926895v1

Connexins Responsible for Hereditary Deafness — The Tale Unfolds

Martine Cohen-Salmon , Francisco del Castillo , Christine Petit
Gap Junctions in Development and Disease, Springer Berlin Heidelberg, pp.111-134, 2005, ⟨10.1007/3-540-28621-7_6⟩
Book sections hal-04028261v1

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

Avital Adato , Gaëlle Lefèvre , Benjamin Delprat , Vincent Michel , Nicolas Michalski , et al.
Human Molecular Genetics, 2005, 14 (24), pp.3921 - 3932. ⟨10.1093/hmg/ddi416⟩
Journal articles pasteur-03926831v1

Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly

Benjamin Delprat , Vincent Michel , Richard Goodyear , Yasuhiro Yamasaki , Nicolas Michalski , et al.
Human Molecular Genetics, 2004, 14 (3), pp.401 - 410. ⟨10.1093/hmg/ddi036⟩
Journal articles istex pasteur-03926836v1

Interactions in the network of Usher syndrome type 1 proteins

Avital Adato , Vincent Michel , Yoshiaki Kikkawa , Jan Reiners , Kumar N Alagramam , et al.
Human Molecular Genetics, 2004, 14, pp.347 - 356. ⟨10.1093/hmg/ddi031⟩
Journal articles istex pasteur-03926828v1