S. Bendahhou
Howard Hughes Medical Institute
Eccles Institute of Human Genetics
University of Utah
Salt Lake City
USA
Name/email consistency: low
- Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5. Bendahhou, S., Cummins, T.R., Kula, R.W., Fu, Y.H., Ptácek, L.J. Neurology (2002)
- Characterization of a new sodium channel mutation at arginine 1448 associated with moderate Paramyotonia congenita in humans. Bendahhou, S., Cummins, T.R., Kwiecinski, H., Waxman, S.G., Ptácek, L.J. J. Physiol. (Lond.) (1999)