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Browsing by Author Monnier, N.

Full Text	Issue Date	Title	Author(s)
	2008	Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores.	Monnier, N.; Marty, I.; Faure, J.; Castiglioni, C.; Desnuelle, C., et al
	1995	Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families	Elbaz, A.; Vale-Santos, J.; Jurkat-Rott, K.; Lapie, P.; Ophoff, R.A., et al