Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22

Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22. https://t.co/ATqCrjbeko

Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22 https://t.co/1rSC5t3mYW

RT @FrontNeurosci: New Research: Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22: Spinocerebellar ataxia 19/22 (SCA19/22)…

New Research: Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22: Spinocerebellar ataxia 19/22 (SCA19/22) is a rare neurodegenerative disorder caused by mutations of the KCND3 gene, which encodes the Kv4. 3… https://t.co/7nYVP3ql7p #Molecula