1-1 of 1
Keywords: DFNA2
Close
Follow your search
Access your saved searches in your account

Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles
Dis Model Mech (2021) 14 (11): dmm049015.
Published: 26 November 2021
...Takashi Kojima; Koichiro Wasano; Satoe Takahashi; Kazuaki Homma ABSTRACT KCNQ4 encodes the homotetrameric voltage-dependent potassium ion channel Kv7.4, and is the causative gene for autosomal dominant nonsyndromic sensorineural hearing loss, DFNA2. Dominant-negative inhibition accounts...
Includes: Supplementary data