(Q55050935)
Statements
A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family. (English)
1 reference
Peter Nürnberg
1 reference
Bernd Wollnik
1 reference
Christian Becker
1 reference
Omar Abidi
1 reference
Abdelhamid Barakat
1 reference
Redouane Boulouiz
1 reference
Abdelaziz Chafik
1 reference
Yun Li
1 reference
Hafid Soualhine
1 reference
Gudrun Nürnberg
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Christian Kubisch
1 reference
1 December 2008
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146A
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23
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3086-3089
1 reference