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Article

Association of TMTC2 With Human Nonsyndromic Sensorineural Hearing Loss.

JAMA otolaryngology-- head & neck surgery - 1 Sept 2016

Runge Christina L, Indap Amit, Zhou Yifan, Kent Jack W, King Ericka, Erbe Christy B, Cole Regina, Littrell Jack, Merath Kate, James Roland, Rüschendorf Franz, Kerschner Joseph E, Marth Gabor, Hübner Norbert, Göring Harald H H, Friedland David R, Kwok Wai-Meng, Olivier Michael

Abstract excerpt

IMPORTANCE: Sensorineural hearing loss (SNHL) is commonly caused by conditions that affect cochlear structures or the auditory nerve, and the genes identified as causing SNHL to date only explain a fraction of the overall genetic risk for this debilitating disorder. It is likely that other genes and mutations also cause SNHL. OBJECTIVE: To identify a candidate gene that causes bilateral, symmetric, progressive...

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Share to Carrier Proteins
Share to Chromosomes, Human, Pair 12

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Disease Progression

Share to Genes, Dominant

Share to Hearing Loss, Bilateral

Share to Hearing Loss, Sensorineural

Share to Membrane Proteins

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Source

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Identifiers

PMID: 27311106
DOI: 10.1001/jamaoto.2016.1444
PMCID: PMC5025373

Genes

TMTC2

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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