Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling.

Source:http://linkedlifedata.com/resource/pubmed/id/20937258

Biochem. Biophys. Res. Commun. 2010 Nov 12 402 2 305-7

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PMID
20937258