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

Source:http://linkedlifedata.com/resource/pubmed/id/17567890

Am. J. Med. Genet. A 2007 Jul 15 143A 14 1592-8

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PMID
17567890