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Article

Identification of novel and known genetic variants associated with hereditary hearing loss in iranian families using whole exome sequencing.

Molecular biology reports - 20 May 2024

Rezaie Nahid, Mansour Samaei Nader, Oladnabi Morteza

Abstract excerpt

BACKGROUND: Hearing loss (HL) is a common sensory impairment worldwide, with genetic and environmental factors contributing to its occurrence. Next Generation Sequencing (NGS) plays a crucial role in identifying the genetic factors involved in this heterogeneous disorder. METHODS AND RESULTS: In this study, a total of 9 unrelated Iranian families, each having at least one affected individual who tested negative...

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Identifiers

PMID: 38767670
DOI: 10.1007/s11033-024-09565-8

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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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