Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain

Tomoko Makishima, Anne C. Madeo, Carmen C. Brewer, Christopher K. Zalewski, John A. Butman, Vandana Sachdev, Andrew E. Arai, Brenda M. Holbrook, Douglas R. Rosing, Andrew J. Griffith

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