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: Takashi Kojima (Author), Koichiro Wasano (Author), Satoe Takahashi (Author), Kazuaki Homma (Author)
Formato: Livro
Publicado em: The Company of Biologists, 2021-11-01T00:00:00Z.
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