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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/38788
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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.date.accessioned2014-05-20T15:29:08Z-
dc.date.accessioned2016-10-25T18:04:21Z-
dc.date.available2014-05-20T15:29:08Z-
dc.date.available2016-10-25T18:04:21Z-
dc.date.issued2005-10-01-
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.urihttp://acervodigital.unesp.br/handle/11449/38788-
dc.format.extent680-680-
dc.language.isoeng-
dc.publisherElsevier B.V.-
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.typeoutro-
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.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.identifier.wosWOS:000232221900028-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofNeuromuscular Disorders-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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