SCN8A mutation in child presenting with...

Molecular Case Studies 2016 / 07

SCN8A mutation in child presenting with seizures and developmental delays

Malcolmson, Janet, Kleyner, Robert, Tegay, David, Adams, Whit, Ward, Kenneth, Coppinger, Justine, Nelson, Lesa, Meisler, Miriam H., Wang, Kai, Robison, Reid, Lyon, Gholson J.
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Language:
english
Journal:
Molecular Case Studies
DOI:
10.1101/mcs.a001073
Date:
July, 2016
File:
PDF, 1.66 MB
english, 2016
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