Screening for mutations in the C-terminal region of RYR1 gene identify high frequency of autosomal recessive form of central core disease (CCD) in Brazil

dc.contributor.authorKossugue, P. M.
dc.contributor.authorMuniz, V. P.
dc.contributor.authorPavanello, RCM
dc.contributor.authorSilva, H. C.
dc.contributor.authorGiannetti, J. G.
dc.contributor.authorPaim, JFO
dc.contributor.authorZatz, M.
dc.contributor.authorVainzof, M.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal de Minas Gerais (UFMG)
dc.contributor.institutionRSHAL
dc.date.accessioned2014-05-20T15:29:08Z
dc.date.available2014-05-20T15:29:08Z
dc.date.issued2005-10-01
dc.description.affiliationIBUSP, Ctr Estudos Genoma Humano, São Paulo, Brazil
dc.description.affiliationUNESP, Dept Anesthesiol, São Paulo, Brazil
dc.description.affiliationUFMG, Belo Horizonte, MG, Brazil
dc.description.affiliationRSHAL, Belo Horizonte, MG, Brazil
dc.description.affiliationUnespUNESP, Dept Anesthesiol, São Paulo, Brazil
dc.format.extent680-680
dc.identifierhttp://www.sciencedirect.com/science/article/pii/S0960896605001884
dc.identifier.citationNeuromuscular Disorders. Oxford: Pergamon-Elsevier B.V., v. 15, n. 9-10, p. 680-680, 2005.
dc.identifier.issn0960-8966
dc.identifier.urihttp://hdl.handle.net/11449/38788
dc.identifier.wosWOS:000232221900028
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofNeuromuscular Disorders
dc.relation.ispartofjcr2.487
dc.relation.ispartofsjr1,337
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.titleScreening for mutations in the C-terminal region of RYR1 gene identify high frequency of autosomal recessive form of central core disease (CCD) in Brazilen
dc.typeResumo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
unesp.author.orcid0000-0003-3970-8025[7]

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