Leukocyte telomere length in patients with transfusion-dependent thalassemia

Abstract Background Thalassemia is a hereditary hemolytic anemia with a severity ranging from mild, non-transfusion dependent to severe chronic anemia requiring lifelong transfusion. Transfusional iron overload is a major complication in patients with transfusion-dependent thalassemia (TDT). Telomer...

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Bibliografski detalji
Glavni autori: Nithita Nanthatanti, Adisak Tantiworawit, Pokpong Piriyakhuntorn, Thanawat Rattanathammethee, Sasinee Hantrakool, Chatree Chai-Adisaksopha, Ekarat Rattarittamrong, Lalita Norasetthada, Wirote Tuntiwechapikul, Kanda Fanhchaksai, Pimlak Charoenkwan, Sirinart Kumfu, Nipon Chattipakorn
Format: Članak
Jezik:English
Izdano: BMC 2020-06-01
Serija:BMC Medical Genomics
Teme:
Online pristup:http://link.springer.com/article/10.1186/s12920-020-00734-9