Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies.
Zhou H; Jungbluth H; Sewry CA; Feng L; Bertini E; Bushby K; Straub V; Roper H; Rose MR; Brockington M; Kinali M; Manzur A; Robb S; Appleton R; Messina S; D'Amico A; Quinlivan R; Swash M; Müller CR; Brown S; Treves S; Muntoni F; Brain: A Journal Of Neurology, 2007, vol. 130, issue Pt 8, p 2024, ISSN 14602156. ISBN 14602156.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef