Dominantly Inherited β-Thalassemia
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260701290092
Reference23 articles.
1. A Genetically Determined Disorder with Features both of Thalassaemia and Congenital Dyserythropoietic Anaemia
2. Inclusion-Body β-Thalassemia Trait
3. Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114
4. One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain [letter]
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1. Dominant inherited β‐thalassemia intermedia in a Polish family due to a novel frameshift mutation in HBB;Pediatric Blood & Cancer;2023-06-23
2. Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT);Hemoglobin;2022-06-10
3. Dominant β-Thalassemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case Report;Hemoglobin;2021-12-27
4. A Randomized, Controlled Study Evaluating the Effects of Silymarin Addition to Deferasirox on the Liver Function of Children with Transfusion-Dependent Thalassemia;Iranian Journal of Pediatric Hematology & Oncology;2021-09-12
5. Thalassemia-Beta major-Case report;Archives of Hematology Case Reports and Reviews;2021-08-12
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