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Article

Absence of KCNQ4 mutation in Bengali families with ADNSHL originated from West Bengal, India.

International journal of pediatric otorhinolaryngology - 1 Sept 2017

Adhikary Bidisha, Bankura Biswabandhu, Biswas Subhradev, Paul Silpita, Das Madhusudan

Abstract excerpt

OBJECTIVE: Autosomal Dominant Non-Syndromic Hearing Loss (ADNSHL) is extremely heterogeneous in nature. More than 60 loci with 30 different genes have been identified linked to ADNSHL. Mutation in KCNQ4 is considered as one of the most common causative factor responsible for ADNSHL. No study focused on the genetic alteration of KCNQ4 gene among hearing loss patients in India. The present study for the first time...

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Source

Identifiers

PMID: 28802383
DOI: 10.1016/j.ijporl.2017.06.004

Genes

KCNQ4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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