The codons 8/9 (+ G) mutation found for the first time in the Lebanese population
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 p...
محفوظ في:
| المؤلف الرئيسي: | |
|---|---|
| مؤلفون آخرون: | , , , |
| التنسيق: | article |
| منشور في: |
2003
|
| الوصول للمادة أونلاين: | http://hdl.handle.net/10725/11115 https://doi.org/10.1081/HEM-120018430 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php https://www.tandfonline.com/doi/full/10.1081/HEM-120018430 |
| الوسوم: |
إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
|
| _version_ | 1864513488283500544 |
|---|---|
| author | Zalloua, Pierre A. |
| author2 | Aoun, Elie Koussa, Suzanne Asfahani, Wissam S.Z. Taher, Ali |
| author2_role | author author author author |
| author_facet | Zalloua, Pierre A. Aoun, Elie Koussa, Suzanne Asfahani, Wissam S.Z. Taher, Ali |
| author_role | author |
| dc.creator.none.fl_str_mv | Zalloua, Pierre A. Aoun, Elie Koussa, Suzanne Asfahani, Wissam S.Z. Taher, Ali |
| dc.date.none.fl_str_mv | 2003 2019-07-22T07:24:36Z 2019-07-22T07:24:36Z 2019-07-22 |
| dc.identifier.none.fl_str_mv | 1532-432X http://hdl.handle.net/10725/11115 https://doi.org/10.1081/HEM-120018430 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. http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php https://www.tandfonline.com/doi/full/10.1081/HEM-120018430 |
| dc.language.none.fl_str_mv | en |
| dc.relation.none.fl_str_mv | Hemoglobin |
| dc.rights.*.fl_str_mv | info:eu-repo/semantics/openAccess |
| dc.title.none.fl_str_mv | The codons 8/9 (+ G) mutation found for the first time in the Lebanese population |
| dc.type.none.fl_str_mv | Article info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/article |
| description | 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. |
| eu_rights_str_mv | openAccess |
| format | article |
| id | LAURepo_d43d3ca2aba1d270ebcbf465748a982a |
| identifier_str_mv | 1532-432X 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. |
| language_invalid_str_mv | en |
| network_acronym_str | LAURepo |
| network_name_str | Lebanese American University repository |
| oai_identifier_str | oai:laur.lau.edu.lb:10725/11115 |
| publishDate | 2003 |
| repository.mail.fl_str_mv | |
| repository.name.fl_str_mv | |
| repository_id_str | |
| spelling | The codons 8/9 (+ G) mutation found for the first time in the Lebanese populationZalloua, Pierre A.Aoun, ElieKoussa, SuzanneAsfahani, Wissam S.Z.Taher, AliThalassemia 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.PublishedN/A2019-07-22T07:24:36Z2019-07-22T07:24:36Z20032019-07-22Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1532-432Xhttp://hdl.handle.net/10725/11115https://doi.org/10.1081/HEM-120018430Zalloua, 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.http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.phphttps://www.tandfonline.com/doi/full/10.1081/HEM-120018430enHemoglobininfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/111152021-03-19T10:47:35Z |
| spellingShingle | The codons 8/9 (+ G) mutation found for the first time in the Lebanese population Zalloua, Pierre A. |
| status_str | publishedVersion |
| title | The codons 8/9 (+ G) mutation found for the first time in the Lebanese population |
| title_full | The codons 8/9 (+ G) mutation found for the first time in the Lebanese population |
| title_fullStr | The codons 8/9 (+ G) mutation found for the first time in the Lebanese population |
| title_full_unstemmed | The codons 8/9 (+ G) mutation found for the first time in the Lebanese population |
| title_short | The codons 8/9 (+ G) mutation found for the first time in the Lebanese population |
| title_sort | The codons 8/9 (+ G) mutation found for the first time in the Lebanese population |
| url | http://hdl.handle.net/10725/11115 https://doi.org/10.1081/HEM-120018430 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php https://www.tandfonline.com/doi/full/10.1081/HEM-120018430 |