Whole-Body muscle MRI in a series of patients with congenital myopathy related to TPM2 gene mutations

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dc.contributor.authorJarraya, M.
dc.contributor.authorQuijano-Roy, S.
dc.contributor.authorMonnier, N.
dc.contributor.authorBéhin, A.
dc.contributor.authorAvila-Smirnov, D.
dc.contributor.authorRomero, N.B.
dc.contributor.authorAllamand, V.
dc.contributor.authorRichard, P.
dc.contributor.authorBarois, A.
dc.contributor.authorMay, A.
dc.contributor.authorEstournet, B.
dc.contributor.authorMercuri, E.
dc.contributor.authorCarlier, P.G.
dc.contributor.authorCarlier, R.-Y.
dc.date.accessioned2023-05-19T20:25:42Z
dc.date.available2023-05-19T20:25:42Z
dc.date.issued2012
dc.fuente.origenORCID-mayo23
dc.identifier.doi10.1016/j.nmd.2012.06.347
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/67462
dc.titleWhole-Body muscle MRI in a series of patients with congenital myopathy related to TPM2 gene mutationses_ES
dc.typeartículo
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