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Filters: Keyword is Genetic Predisposition to Disease and Author is Mohamed Chahine [Clear All Filters]
A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. Neurology. 2016;86(2):161-9.
Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome. Can J Cardiol. 2004;20(4):425-30.