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Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

dc.contributor.authorGarcía Estévez, Daniel Apolinar 
dc.contributor.authorQuintans Castro, Beatriz 
dc.contributor.authorRodrígues de Lemos, Roberta
dc.date.accessioned2017-06-07T07:10:57Z
dc.date.available2017-06-07T07:10:57Z
dc.date.issued2013
dc.identifier.issn1364-6745
dc.identifier.urihttp://hdl.handle.net/20.500.11940/3548
dc.language.isoeng
dc.titleMutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
dc.typeArtigoes
dc.authorsophosHsu, S. C.
dc.authorsophosSears, R. L.
dc.authorsophosLemos, R. R.
dc.authorsophosQuintáns, B.
dc.authorsophosHuang, A.
dc.authorsophosSpiteri, E.
dc.authorsophosNevarez, L.
dc.authorsophosMamah, C.
dc.authorsophosZatz, M.
dc.authorsophosPierce, K. D.
dc.authorsophosFullerton, J. M.
dc.authorsophosAdair, J. C.
dc.authorsophosBerner, J. E.
dc.authorsophosBower, M.
dc.authorsophosBrodaty, H.
dc.authorsophosCarmona, O.
dc.authorsophosDobricić, V.
dc.authorsophosFogel, B. L.
dc.authorsophosGarcía-Estevez, D.
dc.authorsophosGoldman, J.
dc.authorsophosGoudreau, J. L.
dc.authorsophosHopfer, S.
dc.authorsophosJanković, M.
dc.authorsophosJaumà, S.
dc.authorsophosJen, J. C.
dc.authorsophosKirdlarp, S.
dc.authorsophosKlepper, J.
dc.authorsophosKostić, V.
dc.authorsophosLang, A. E.
dc.authorsophosLinglart, A.
dc.authorsophosMaisenbacher, M. K.
dc.authorsophosManyam, B. V.
dc.authorsophosMazzoni, P.
dc.authorsophosMiedzybrodzka, Z.
dc.authorsophosMitarnun, W.
dc.authorsophosMitchell, P. B.
dc.authorsophosMueller, J.
dc.authorsophosNovaković, I.
dc.authorsophosPaucar, M.
dc.authorsophosPaulson, H.
dc.authorsophosSimpson, S. A.
dc.authorsophosSvenningsson, P.
dc.authorsophosTuite, P.
dc.authorsophosVitek, J.
dc.authorsophosWetchaphanphesat, S.
dc.authorsophosWilliams, C.
dc.authorsophosYang, M.
dc.authorsophosSchofield, P. R.
dc.authorsophosDe Oliveira, J. R. M.
dc.authorsophosSobrido, M. J.
dc.authorsophosGeschwind, D. H.
dc.authorsophosCoppola, G.
dc.identifier.doi10.1007/s10048-012-0349-2
dc.identifier.isi314762500002
dc.identifier.pmid23334463
dc.identifier.sophos13290
dc.issue.number1
dc.journal.titleNEUROGENETICS
dc.organizationConsellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Lugo - Hospital Comarcal de Monforte::Neuroloxía
dc.page.initial11
dc.page.final22
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number14


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