A Patient with β-Thalassemia Intermedia Secondary to Homozygosity for a Polyadenylation Signal Mutation (AATAAA > AATAGA) (HBB: C.*112A > G) on the β-Globin Gene

Yen-Chian LimDepartment of Haematology, Tan Tock Seng Hospital, Singapore; Correspondence[email protected]

Karen M.L. TanMolecular Diagnosis Centre, Department of Laboratory Medicine, National University Hospital, Singapore;

Samuel S. ChongMolecular Diagnosis Centre, Department of Laboratory Medicine, National University Hospital, Singapore; ;Department of Paediatrics, Yong Loo Lin School of Medicine, National University Singapore, Singapore

Joseph RajendranDepartment of Haematology, Tan Tock Seng Hospital, Singapore;

Venkatasreekanth SampathDepartment of Haematology, Tan Tock Seng Hospital, Singapore;

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Faten Haddad, Nawel Trabelsi, Leila Chaouch, Imen Darragi, Meriem Oueslati, Imen Boudriga, Dorra Chaouachi, Wijdene El-Borgi, Raouf Hafsia, Salem Abbes & Houyem Ouragini. (2017) Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert’s Syndrome. Hemoglobin 41:2, pages 147-150.
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Adivitch Sripusanapan, Arunee Phusua, Kanda Fanhchaksai & Pimlak Charoenkwan. (2020) Compound heterozygosity of a silent beta‐thalassemia mutation at the 3′‐untranslated region ( HBB : c.*132 C>T) and beta‐zero thalassemia results in thalassemia intermedia . Pediatric Blood & Cancer 67:4.
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A Patient with β-Thalassemia Intermedia Secondary to Homozygosity for a Polyadenylation Signal Mutation (AATAAA > AATAGA) (HBB: C.*112A > G) on the β-Globin Gene

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A Patient with β-Thalassemia Intermedia Secondary to Homozygosity for a Polyadenylation Signal Mutation (AATAAA > AATAGA) (HBB: C.*112A > G) on the β-Globin Gene

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