Common fetal hemoglobin variants in Lebanese patients bearing the codon 29 beta gene mutation associated with different thalassemia phenotypes-Reference-Cited by-同舟云学术

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Common fetal hemoglobin variants in Lebanese patients bearing the codon 29 beta gene mutation associated with different thalassemia phenotypes

Published:2018-11-30 Issue:4 Volume:98 Page:833-840
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Brancaleoni Valentina,Moukhadder Hassan M.,Consonni Dario,Koussa Suzanne,Di Pierro Elena,Cappellini Maria Domenica,Taher Ali

Funder

Italian Ministry of Health and Fondazione IRCCS Ca’ Granda

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00277-018-3567-3.pdf

Reference18 articles.

1. Taher AT, Weatherall DJ, Cappellini MD (2018) Thalassaemia. Lancet 391:155–167 β-globin

2. Galanello R, Cao A (1998) Relationship between genotype and phenotype. Thalassemia intermedia. Ann N Y Acad Sci 850:325–333

3. Taher A, Isma'eel H, Cappellini MD (2006) Thalassemia intermedia: revisited. Blood Cells Mol Dis 37:12–20

4. Danjou F, Anni F, Perseu L, Satta S, Dessi C, Lai ME, Fortina P, Devoto M, Galanello R (2012) Genetic modifiers of beta-thalassemia and clinical severity as assessed by age at first transfusion. Haematologica 97:989–993

5. Labie D, Dunda-Belkhodja O, Rouabhi F, Pagnier J, Ragusa A, Nagel RL (1985) The −158 site 5′ to the G gamma gene and G gamma expression. Blood 66:1463–1465

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Foetal haemoglobin elevation, unfavourable prognosis, and protective role of genetic variants HBG2 rs7482144, HBS1L-MYB rs9399137 and BCL11A rs4671393 in children with ALL;Journal of Genetics;2024-04-17

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