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A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family
Author(s) -
Boulouiz Redouane,
Li Yun,
Soualhine Hafid,
Abidi Omar,
Chafik Abdelaziz,
Nürnberg Gudrun,
Becker Christian,
Nürnberg Peter,
Kubisch Christian,
Wollnik Bernd,
Barakat Abdelhamid
Publication year - 2008
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.32525
Subject(s) - genetics , medicine , library science , humanities , biology , art , computer science
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