Case series of homozygous and compound heterozygosity of Hb Malay, the diagnostic features and transfusion requirements
Hb Malay was first described in 1989 following an investigation of anaemia in a 22-year-old Malay gentleman who was homozygous for this b chain variant. This Hb variant is caused by AAC à AGC mutation at codon 19 of the b globin gene resulting in the substitution of serine for asparagine [1]. The mu...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Advanced Medical and Dental Institute (AMDI)
2017
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| Online Access: | http://psasir.upm.edu.my/id/eprint/61055/1/Case%20series%20of%20homozygous%20and%20compound%20heterozygosity%20of%20Hb%20Malay%2C%20the%20diagnostic%20features%20and%20transfusion%20requirements.pdf http://psasir.upm.edu.my/id/eprint/61055/ http://apps.amdi.usm.my/journal/index.php/jbcs/article/view/131 |
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