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Browsing by Author Estournet, B.

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