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Article

Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.

Journal of medical genetics - 1 Aug 2006

Shabbir M I, Ahmed Z M, Khan S Y, Riazuddin Saima, Waryah A M, Khan S N, Camps R D, Ghosh M, Kabra M, Belyantseva I A, Friedman T B, Riazuddin Sheikh

Abstract excerpt

BACKGROUND: Approximately half the cases of prelingual hearing loss are caused by genetic factors. Identification of genes causing deafness is a crucial first step in understanding the normal function of these genes in the auditory system. Recently, a mutant allele of Tmhs was reported to be associated with deafness and circling behaviour in the hurry-scurry mouse. Tmhs encodes a predicted tetraspan protein of...

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Share to Chromosomes, Human, Pair 6
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Recessive

Share to Hair Cells, Auditory, Inner

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Source

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Identifiers

PMID: 16459341
DOI: 10.1136/jmg.2005.039834
PMCID: PMC2564584

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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