Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia-Reference-Cited by-同舟云学术

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Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia

Published:2018-03-04 Issue:2 Volume:42 Page:96-102
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Belhaj Nefissi Rim¹,Doggui Radhouene²,Ouali Faida³,Messaoud Taieb³,Gritli Nasreddine¹

Affiliation:

1. Laboratory of Molecular Biology, Department of Hematology, Military Hospital of Tunis, Tunisia;

2. Laboratory of Biochemistry and Molecular Biology, Children’s Hospital of Tunis, Tunisia;

3. National Institute of Nutrition and Food Technology (INNTA) Tunis, Tunisia

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2018.1451340

Reference44 articles.

1. Sickle Cell Anemia, a Molecular Disease

2. SICKLE CELL ANEMIA

3. SICKLE CELL DISEASE

4. Sickle Cell Hemoglobin Polymerization

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1. Thromboembolism in Children;Indian Journal of Pediatrics;2023-05-05

2. Common Thrombophilic Mutations among Sickle Cell Disease Patients in the Western Province of Saudi Arabia;INT J HUM GENET;2023

3. Relevance of Plasma Homocysteine and Methylenetetrahydrofolate Reductase 677TT Genotype in Sickle Cell Disease: A Systematic Review and Meta-Analysis;International Journal of Molecular Sciences;2022-11-24

4. Thrombophilic mutations and risk of vascular complications in sickle cell disease;Gene Reports;2022-06

5. MTHFR C677T, Prothrombin G20210A, and Factor V Leiden (G1691A) Polymorphism and Beta-Thalassemia Risk: A Meta-Analysis;Cureus;2020-09-30

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