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The large Chinese family with Y-linked hearing loss revisited: clinical investigation.

Acta oto-laryngologica - 1 Jun 2009

Wang Qiu-Ju, Rao Shao-Qi, Zhao Ya-Li, Liu Qing-Jie, Zong Liang, Han Ming-Kun, Han Dong-Yi, Yang Wei-Yan

Abstract excerpt

CONCLUSION: The DFNY1 phenotypes shared many characteristics with some autosomal dominant hearing loss, in the aspects of age of onset, severity and audiometric configuration. However, the typical, outstanding feature of this trait was its remarkable pattern of inheritance. Similar traits, if ever encountered, can be most easily identified by discerning this exceptional and rare pattern of inheritance....

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PMID: 18720061
DOI: 10.1080/00016480802216347

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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