Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss
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 for the observed dominant inheritance of many DFNA2-associated KCNQ4 variants. In add...
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| Main Authors: | , , , |
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| Format: | Book |
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The Company of Biologists,
2021-11-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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