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A Novel Dfnb31 Mutation Associated with Usher Type 2 Syndrome Showing Variable Degrees of Auditory Loss in A Consanguineous Portuguese Family.

Isabelle Audo,Kinga Bujakowska,Saddek Mohand-Said,Sophie Tronche,Marie-Elise Lancelot,Aline Antonio,Aurore Germain,Christine Lonjou,Wassila Carpentier,Jose-Alain Sahel,Shomi Bhattacharya,Christina Zeitz

MOLECULAR VISION（2011）

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关键词
novel dfnb31 mutation,auditory loss,usher type,consanguineous portuguese family,syndrome
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