Clinical and laboratory features of Hemoglobin La Desirade variant in association with sickle cell and alpha thalassemia genes

Autor: Alkindi, S., Al Zadjali, S., Al Rawahi, M., Al Haddabi, H., Daar, S., ElSadek, R.A., Sherkawy, B.D., Pathare, A.V.

Publikováno v: Mediterranean Journal of Hematology and Infectious Diseases, Vol 13, Iss 1 (2021)
Mediterranean Journal of Hematology and Infectious Diseases

Hemoglobin La Desirade (Hb La Desirade) is an unstable hemoglobin variant characterized by amino acid Alanine (Ala) replacing Valine (Val) at position 129 (H7) in the beta chain. Hb La Desirade exhibits a decreased oxygen affinity and normal heme-hem

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5350df4da2ad63f3cecfeff5daa00a83
http://www.mjhid.org/index.php/mjhid/article/view/4419