Export 2 results:
Filters: Keyword is DNA Mutational Analysis [Clear All Filters]
Y1767C, a novel SCN5A mutation, induces a persistent Na+ current and potentiates ranolazine inhibition of Nav1.5 channels. Am J Physiol Heart Circ Physiol. 2011;300(1):H288-99.
Autosomal dominant macular dystrophy in a large Canadian family. Can J Ophthalmol. 2003;38(1):33-40.