dc.contributor.author |
Zalloua, Pierre A. |
|
dc.contributor.author |
Aoun, Elie |
|
dc.contributor.author |
Koussa, Suzanne |
|
dc.contributor.author |
Asfahani, Wissam S.Z. |
|
dc.contributor.author |
Taher, Ali |
|
dc.date.accessioned |
2019-07-22T07:24:36Z |
|
dc.date.available |
2019-07-22T07:24:36Z |
|
dc.date.copyright |
2003 |
en_US |
dc.date.issued |
2019-07-22 |
|
dc.identifier.issn |
1532-432X |
en_US |
dc.identifier.uri |
http://hdl.handle.net/10725/11115 |
|
dc.description.abstract |
Thalassemia is a common inherited disease in the Mediterranean region. We here report a mutation new to the Lebanese population: the insertion of a G nucleotide at codons 8/9 [(+G) AAG‐TCT (Lys‐Ser)→AAG‐G‐TCT (β0)] of the β‐globin gene in a thalassemic patient with a mild phenotype. We discuss the possible factors that play a role in alleviating the severity of the disease in this case. |
en_US |
dc.language.iso |
en |
en_US |
dc.title |
The codons 8/9 (+ G) mutation found for the first time in the Lebanese population |
en_US |
dc.type |
Article |
en_US |
dc.description.version |
Published |
en_US |
dc.author.school |
SOM |
en_US |
dc.author.idnumber |
20030001 |
en_US |
dc.author.department |
N/A |
en_US |
dc.description.embargo |
N/A |
en_US |
dc.relation.journal |
Hemoglobin |
en_US |
dc.journal.volume |
27 |
en_US |
dc.journal.issue |
1 |
en_US |
dc.article.pages |
1-5 |
en_US |
dc.identifier.doi |
https://doi.org/10.1081/HEM-120018430 |
en_US |
dc.identifier.ctation |
Zalloua, P. A., Aoun, E., Koussa, S., Asfahani, W. S., & Taher, A. (2003). The codons 8/9 (+ G) mutation found for the first time in the Lebanese population. Hemoglobin, 27(1), 1-5. |
en_US |
dc.author.email |
pierre.zalloua@lau.edu.lb |
en_US |
dc.identifier.tou |
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php |
en_US |
dc.identifier.url |
https://www.tandfonline.com/doi/full/10.1081/HEM-120018430 |
en_US |
dc.orcid.id |
https://orcid.org/0000-0002-8494-5081 |
en_US |
dc.author.affiliation |
Lebanese American University |
en_US |