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Article

Novel OTOF gene mutations identified using a massively parallel DNA sequencing technique in DFNB9 deafness.

Acta oto-laryngologica - 1 Oct 2018

Wang Yanfei, Lu Yu, Cheng Jing, Zhang Lei, Han Dongyi, Yuan Huijun

Abstract excerpt

OBJECTIVES: This study examined the causative genes in patients with early-onset hearing loss from two Chinese families. METHOD: Massively parallel sequencing, designed to screen all reported genes associated with hearing loss, was performed in a large number of Chinese individuals with hearing loss. This study enrolled patients with the same OTOF mutation and analyzed their phenotype-genotype correlations....

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Identifiers

PMID: 30073893
DOI: 10.1080/00016489.2018.1476777

Genes

OTOF

Variants

Provenance

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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