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Identification of a novel deletion in UDP-glucuronosyltransferase gene in a patient with Crigler-Najjar syndrome type I

dc.contributor.authorCosta, Elisio
dc.contributor.authorVieira, Emilia
dc.contributor.authordos Santos, Rosario
dc.contributor.authorLopes, Ana Isabel
dc.contributor.authorSaldanha, Maria Joana
dc.contributor.authorBrites, Dora
dc.date.accessioned2015-12-30T10:18:24Z
dc.date.available2015-12-30T10:18:24Z
dc.date.issued2009
dc.formatapplication/pdf
dc.identifier.citationBLOOD CELLS MOLECULES AND DISEASES. - Vol. 42, n. 3 (MAY-JUN 2009), p. 265-266
dc.identifier.doihttp://dx.doi.org/10.1016/j.bcmd.2008.12.004
dc.identifier.issn1079-9796
dc.identifier.urihttp://hdl.handle.net/10451/21575
dc.language.isoeng
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE
dc.subjectHematology
dc.titleIdentification of a novel deletion in UDP-glucuronosyltransferase gene in a patient with Crigler-Najjar syndrome type I
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage266por
oaire.citation.startPage265por
oaire.citation.titleBLOOD CELLS MOLECULES AND DISEASESpor
oaire.citation.volumeVol. 42por
rcaap.rightsrestrictedAccess
rcaap.typearticle

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