Novel mutation in alpha-spectrin gene in Saudi patients with hereditary spherocytosis-Reference-Cited by-同舟云学术

Novel mutation in alpha-spectrin gene in Saudi patients with hereditary spherocytosis

Published:2024-02-06 Issue: Volume: Page:1-20
ISSN:1525-7770
Container-title:Nucleosides, Nucleotides & Nucleic Acids
language:en
Short-container-title:Nucleosides, Nucleotides & Nucleic Acids

Author:

Alshomar Ahmad¹^ORCID,Ahmed Ahmed A.²,Rasheed Zafar³^ORCID,Alhumaydhi Fahad A.⁴^ORCID,Alsagaby Suliman⁵,Aljohani Abdullah S. M.⁶^ORCID,Alkhamiss Abdullah S.³,Alghsham Ruqaih³^ORCID,Althwab Sami A.⁷,Khan Muhammad Ismail⁸,Fernández Nelson⁹,Al Abdulmonem Waleed³^ORCID

Affiliation:

1. Department of Medicine, College of Medicine, Qassim University, Buraidah, Saudi Arabia

2. Research Center, College of Medicine, Qassim University, Buraidah, Saudi Arabia

3. Department of Pathology, College of Medicine, Qassim University, Buraidah, Saudi Arabia

4. Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraidah, Saudi Arabia

5. Department of Medical Laboratories Sciences, College of Applied Medical Sciences, Majmaah University, Majmaah, Saudi Arabia

6. Department of Veterinary Medicine, College of Agricultural and Veterinary Medicine, Qassim University, Buraydah, Saudi Arabia

7. Department of Food Science and Human Nutrition, College of Agriculture and Veterinary Medicine, Qassim University, Buraidah, Saudi Arabia

8. Faculty of Medicine, School of Public Health, University of Queensland, Brisbane, Australia

9. School of Life Sciences, University of Essex, Colchester, UK

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/15257770.2024.2310703

Reference31 articles.

1. The molecular basis of hereditary red cell membrane disorders

2. Hereditary red cell membrane disorders and laboratory diagnostic testing

3. Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin

4. Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients

5. An Infant With Unusually High Unconjugated Hyperbilirubinemia Due to Coexistence of Hereditary Spherocytosis and Gilbert Syndrome