A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] With Other α-Thalassemias in Malay Families

Hafiza AlauddinHaematology Unit, Department of Pathology, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysiaCorrespondence[email protected]

Noor-Adilah JaaparHaematology Unit, Department of Pathology, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia

Raja Z. AzmaHaematology Unit, Department of Pathology, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia

Azlin IthninHaematology Unit, Department of Pathology, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia

Noor-Farisah A. RazakDiagnostic Medical Laboratory Department, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia

C-Khai LohDepartment of Paediatrics, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia

Hamidah AliasDepartment of Paediatrics, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia

Zarina Abdul-LatiffDepartment of Paediatrics, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia

Ainoon OthmanDepartment of Medical Science II, Faculty of Medicine and Health Science, Universiti Sains Islam NilaiMalaysia

show all

A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] With Other α-Thalassemias in Malay Families

Information for

Open access

Opportunities

Help and information

Your download is now in progress and you may close this window

Login or register to access this feature

A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] With Other α-Thalassemias in Malay Families

Reprints and Corporate Permissions

Academic Permissions

Related research

To cite this article:

Download citation

Information for

Open access

Opportunities

Help and information

Keep up to date