Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 205,231,728 papers from all fields of science
Search
Sign In
Create Free Account
GRXCR2 gene
Known as:
DFNB101
, GRXCR2
, glutaredoxin and cysteine rich domain containing 2
Expand
National Institutes of Health
Create Alert
Alert
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
A. Imtiaz
,
D. Kohrman
,
S. Naz
Human mutation
2014
Corpus ID: 19845589
More than 360 million humans are affected with some degree of hearing loss, either early or later in life. A genetic cause for…
Expand
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