LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss.

This study, which describes a novel LHFPL5 mutation in a family of Omani origin with hereditary hearing loss, supports previous clinical descriptions of the condition and contributes to the genetic spectrum of mutations in this form of deafness. PMID: 30476627 [PubMed - as supplied by publisher] (Source: European Journal of Medical Genetics)

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