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Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutations

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author: Vincent Morinière  Corinne Antignac  Laurence Heidet  Dominique Bonneau 

Publication date January 28, 2011
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