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dc.contributor.authorMohamad, A.S.-
dc.contributor.authorHamzah, R.-
dc.contributor.authorSelvaratnam, V.-
dc.contributor.authorYegapan, S.-
dc.contributor.authorSathar, J.-
dc.date.accessioned2019-11-29T09:36:03Z-
dc.date.available2019-11-29T09:36:03Z-
dc.date.issued2018-09-
dc.identifier.citationMohamad, A. S., Hamzah, R., Selvaratnam, V., Yegapan, S., & Sathar, J. (2018). Human hemoglobin G-Makassar variant masquerading as sickle cell anemia. Hematology Reports, 10(3), 92–95.en_US
dc.identifier.issn20388322-
dc.identifier.urihttps://doi.org/10.4081/hr.2018.7210-
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176384/-
dc.identifier.urihttp://ir.unikl.edu.my/jspui/handle/123456789/23248-
dc.descriptionThis is an open access article distributed under the terms of the Creative Commons CC-BY license. This article index by Scopusen_US
dc.description.abstractHuman hemoglobin of G-Makassar variant has been reported very rarely with Beta Thalassemia. In year 1969 Hb GMakassar was first identified in Makassar, Sulawesi (Celebes), Republic of Indonesia. The disease was first published in 1969 and 33 years later it has been reported at a family of Thailand origin. We report a 45-yearold Malay man who was investigated for anemia and thrombocytopenia then diagnosed with Hb G-Makassar. This finding describes as a new Hemoglobin GMakassar discovered in Malaysia after 14 years diagnosed in Thailand.en_US
dc.language.isoenen_US
dc.publisherPage Press Publicationsen_US
dc.subjectHemoglobin G-Makassaren_US
dc.subjectelectrophoresisen_US
dc.subjectbeta thalassemiaen_US
dc.subjectDNA analysisen_US
dc.subjectsickle cell diseaseen_US
dc.titleHuman hemoglobin G-Makassar variant masquerading as sickle cell anemiaen_US
dc.typeArticleen_US
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