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Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719C.

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author: Redouane Boulouiz  Abdelaziz Chafik  Abdelhamid Barakat  Christian Kubisch  Omar Abidi  Bernd Wollnik 

Publication date October 2, 2007
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