Skip to search formSkip to main contentSkip to account menu

DEAFNESS, AUTOSOMAL RECESSIVE 26

Known as: DFNB26 
National Institutes of Health

Related topics

Related topics

3 relations
Autosomal recessive inheritanceDFNB26 geneSensorineural Hearing Loss (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Modifier variant of METTL13 suppresses human GAB1–associated profound deafness
A modifier variant can abrogate the risk of a monogenic disorder. DFNM1 is a locus on chromosome 1 encoding a dominant suppressor… 
Highly Cited
2000
Highly Cited
2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26
More than 50% of severe childhood deafness is genetically determined, approximately 70% of which occurs without other… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)