Varaico: Literature-Extracted Genetic Variants

Gene:COCH
Variant:p.L56delFs
Back to variants list

COCH

NM_004086.3:p.L56delFs

Associated Papers

Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta-analysis.

Aliazami F et al.

International Journal of Pediatric Otorhinolaryngology, 2023

The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients.

Usami SI et al.

Human Genetics, 2022

Genetic investigations in childhood deafness.

Parker M et al.

Archives of Disease in Childhood, 2015

Genetics of hearing and deafness.

Angeli S et al.

Anatomical Record (hoboken, N.j. : 2007), 2012

Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis.

Schrijver I et al.

Expert Review of Molecular Diagnostics, 2006

Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound.

Schrijver I

The Journal of Molecular Diagnostics : Jmd, 2004

Molecular genetics of hearing loss.

Petit C et al.

Annual Review of Genetics, 2001

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."