Show simple item record

dc.contributor.authorFinlayson, J.
dc.contributor.authorGhassemifar, Reza
dc.contributor.authorHolmes, P.
dc.contributor.authorGrey, D.
dc.contributor.authorFigliomeni, L.
dc.contributor.authorNewbound, C.
dc.contributor.authorPell, N.
dc.contributor.authorKersten, M.
dc.contributor.authorJennens, M.
dc.contributor.authorMacaulay, C.
dc.contributor.authorGreenwood, L.
dc.contributor.authorBeilby, J.
dc.date.accessioned2017-01-30T12:44:39Z
dc.date.available2017-01-30T12:44:39Z
dc.date.created2016-09-12T08:36:53Z
dc.date.issued2010
dc.identifier.citationFinlayson, J. and Ghassemifar, R. and Holmes, P. and Grey, D. and Figliomeni, L. and Newbound, C. and Pell, N. et al. 2010. Hb East Timor [ß80(EF4)Asn?His, AAC>CAC (HBB c.241A>C)], a variant hemoglobin associated with normal hematology. Hemoglobin. 34 (6): pp. 561-564.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/24726
dc.identifier.doi10.3109/03630269.2010.526896
dc.description.abstract

Routine hemoglobin (Hb) analyses identified a new ß-globin variant in a family from East Timor. The red cell indices were within normal limits for all affected family members. The variant is due to a missense mutation at amino acid codon 80 (AAC>CAC) which results in the substitution of histidine for asparagine. © 2010 Informa Healthcare USA, Inc.

dc.publisherTaylor and Francis Ltd
dc.titleHb East Timor [ß80(EF4)Asn?His, AAC>CAC (HBB c.241A>C)], a variant hemoglobin associated with normal hematology
dc.typeJournal Article
dcterms.source.volume34
dcterms.source.number6
dcterms.source.startPage561
dcterms.source.endPage564
dcterms.source.issn0363-0269
dcterms.source.titleHemoglobin
curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusFulltext not available


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record