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Gaucher disease in Tunisia: High frequency of the most common mutations

dc.contributor.authorCherif, W.
dc.contributor.authorBen Turkia, H.
dc.contributor.authorBen Rhouma, F.
dc.contributor.authorRiahi, I.
dc.contributor.authorChemli, J.
dc.contributor.authorKefi, R.
dc.contributor.authorMessai, H.
dc.contributor.authorAmaral, O.
dc.contributor.authorMiranda, M.C.
dc.contributor.authorCaillaud, C.
dc.contributor.authorTebib, N.
dc.contributor.authorBen Dridi, M.F.
dc.contributor.authorAbdelhak, S.
dc.date.accessioned2011-10-27T11:57:57Z
dc.date.available2011-10-27T11:57:57Z
dc.date.issued2009-09
dc.identifier.citationBlood Cells Mol Dis. 2009 Sep-Oct;43(2):161-2. Epub 2009 Jun 23por
dc.identifier.issn1079-9796
dc.identifier.otherdoi:10.1016/j.bcmd.2009.05.004
dc.identifier.urihttp://hdl.handle.net/10400.18/301
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S1079979609001338por
dc.subjectGaucher disease/epidemiologypor
dc.subjectGenetic diseasespor
dc.subjectHuman Geneticspor
dc.subjectTunisiapor
dc.subjectDoenças genéticaspor
dc.subjectLysosomal Storage Diseasepor
dc.titleGaucher disease in Tunisia: High frequency of the most common mutationspor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage162por
oaire.citation.startPage161por
oaire.citation.titleBlood Cells, Molecules and Diseasespor
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor

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