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KCNQ4, GLY321SER

 
National Institutes of Health

Papers overview

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2019
2019
Variants of KCNQ4 are one of the most common causes of dominantly inherited nonsyndromic hearing loss. We investigated a… Expand
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2008
2008
KCNQ1-5 (Kv7.1-7.5) subunits assemble to form a variety of functional K(+) channels in the nervous system, heart, and epithelia… Expand
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