https://nsc89303.com/embedding....-covariate-adjustmen
Objective Numerous pathogenic alternatives in KCNB1, which encodes the voltage-gated potassium channel, KV2.1, are linked to developmental and epileptic encephalopathies and associated with loss-of-function, -regulation, and -expression associated with the channel. Right here we describe a novel de novo variant (P17T) occurring into the KV2.1 station that is related to a gain-of-function (GoF), with changed steady-state inactivation and paid off sensitiveness towards the selective
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