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Keywords: DFNA2
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Journal Articles
In collection:
Human Genetic Disease
Journal:
Disease Models & Mechanisms
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