A1152D mutation of the Na+ channel causes paramyotonia...

The Journal of Physiology 2005 Vol. 565; Iss. 2

A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4–S5 linker in fast inactivation

Magali Bouhours, Sandrine Luce, Damien Sternberg, Jean Claude Willer, Bertrand Fontaine, Nacira Tabti
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Volume:
565
Year:
2005
Language:
english
Pages:
13
DOI:
10.1113/jphysiol.2004.081018
File:
PDF, 402 KB
english, 2005
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