Structural and functional analysis of the ASM p.Ala359Asp mutant that causes acid sphingomyelinase deficiency

dc.contributor.authorAcuña, Mariana
dc.contributor.authorCastro Fernández, Víctor
dc.contributor.authorLatorre, Mauricio
dc.contributor.authorCastro, Juan
dc.contributor.authorSchuchman, Edward H.
dc.contributor.authorGuixé, Victoria
dc.contributor.authorGonzález, Mauricio
dc.contributor.authorZanlungo Matsuhiro, Silvana
dc.date.accessioned2020-08-13T21:25:16Z
dc.date.available2020-08-13T21:25:16Z
dc.date.issued2016
dc.format.extent6 páginas
dc.fuente.origenConveris
dc.identifier.doi10.1016/j.bbrc.2016.09.096
dc.identifier.issn0006-291X
dc.identifier.issn1090-2104
dc.identifier.urihttps://doi.org/10.1016/j.bbrc.2016.09.096
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/38607
dc.issue.numeroNo. 3
dc.language.isoen
dc.nota.accesoContenido parcial
dc.pagina.final501
dc.pagina.inicio496
dc.revistaBiochemical and Biophysical Research Communicationses_ES
dc.rightsacceso restringido
dc.subject.ddc610
dc.subject.deweyMedicina y saludes_ES
dc.subject.otherEnfermedad de Niemann-Pickes_ES
dc.subject.otherEnfermedades hereditariases_ES
dc.subject.otherFibroblastoses_ES
dc.titleStructural and functional analysis of the ASM p.Ala359Asp mutant that causes acid sphingomyelinase deficiencyes_ES
dc.typeartículo
dc.volumenVol. 479
sipa.codpersvinculados72650
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