Human hemoglobin G-Makassar variant masquerading as sickle cell anemia

Mohamad, A.S.; Hamzah, R.; Selvaratnam, V.; Yegapan, S.; Sathar, J.

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dc.contributor.author	Mohamad, A.S.
dc.contributor.author	Hamzah, R.
dc.contributor.author	Selvaratnam, V.
dc.contributor.author	Yegapan, S.
dc.contributor.author	Sathar, J.
dc.date.accessioned	2019-11-29T09:36:03Z
dc.date.available	2019-11-29T09:36:03Z
dc.date.issued	2018-09
dc.identifier.citation	Mohamad, 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.issn	20388322
dc.identifier.uri	https://doi.org/10.4081/hr.2018.7210
dc.identifier.uri	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176384/
dc.identifier.uri	http://ir.unikl.edu.my/jspui/handle/123456789/23248
dc.description	This is an open access article distributed under the terms of the Creative Commons CC-BY license. This article index by Scopus	en_US
dc.description.abstract	Human 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.iso	en	en_US
dc.publisher	Page Press Publications	en_US
dc.subject	Hemoglobin G-Makassar	en_US
dc.subject	electrophoresis	en_US
dc.subject	beta thalassemia	en_US
dc.subject	DNA analysis	en_US
dc.subject	sickle cell disease	en_US
dc.title	Human hemoglobin G-Makassar variant masquerading as sickle cell anemia	en_US
dc.type	Article	en_US