Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvβ1.1 and Kv1.4-1.1/Kvβ1.2

Paola Imbrici, Maria Cristina D'Adamo, Dimitri M. Kullmann, Mauro Pessia

Research output: Contribution to journal › Article › peer-review

46 Citations (Scopus)

Fingerprint

Dive into the research topics of 'Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvβ1.1 and Kv1.4-1.1/Kvβ1.2'. Together they form a unique fingerprint.

Medicine & Life Sciences