SCN4A pore mutation pathogenetically contributes to...

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Human Molecular Genetics 2015 / 10

SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy

Bergareche, Alberto, Bednarz, Marcin, Sánchez, Elena, Krebs, Catharine E., Ruiz-Martinez, Javier, De la Riva, Patricia, Makarov, Vladimir, Gorostidi, Ana, Jurkat-Rott, Karin, Marti-Masso, Jose Felix,
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Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddv410
Date:
October, 2015
File:
PDF, 1013 KB
english, 2015
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