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Article

A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss

4 May 2015

Abstract excerpt

BACKGROUND: Hearing loss is a heterogeneous neurosensory disorder. Mutations of 56 genes are reported to cause recessively inherited non-syndromic deafness. OBJECTIVE: We sought to identify the genetic lesion causing hearing loss segregating in a large consanguineous Pakistani family. METHODS AND RESULTS: Mutations of GJB2 and all other genes reported to underlie recessive deafness were ruled out as the cause of...

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PMID: 25941349
DOI: 10.1136/jmedgenet-2015-103023

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