Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

GRXCR2 gene

Known as: DFNB101, GRXCR2, glutaredoxin and cysteine rich domain containing 2 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
A Frameshift Mutation in GRXCR2 Causes Recessively Inherited Hearing Loss
More than 360 million humans are affected with some degree of hearing loss, either early or later in life. A genetic cause for… Expand
Is this relevant?
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE