Additional file 2: Figure S2.

Pedigrees of 11 families with ARNSHL. All families comprised normally hearing parents and two affected siblings. Asterisks indicate sequenced sample. Two (A and B) of 11 families had causative MYO15A mutation [18]. In the other families (C-K), the causative mutations in known deafness genes were not identified.

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Woo et al. BMC Medical Genetics 2014 15:46   doi:10.1186/1471-2350-15-46