Recent progress in laboratory diagnosis of thalassemia and hemoglobinopathy: a study by the Korean Red Blood Cell Disorder Working Party of the Korean Society of Hematology

Genetic hemoglobin disorders are caused by mutations and/or deletions in the α-globin or β-globin genes. Thalassemia is caused by quantitative defects and hemoglobinopathies by structural defect of hemoglobin. The incidence of thalassemia and hemoglobinopathy is increased in Korea with rapid influx...

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Detalles Bibliográficos
Autores principales: Lee, Young Kyung, Kim, Hee-Jin, Lee, Kyunghoon, Park, Sang Hyuk, Song, Sang Hoon, Seong, Moon-Woo, Kim, Myungshin, Han, Jin Yeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2019
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439293/
https://www.ncbi.nlm.nih.gov/pubmed/30956959
http://dx.doi.org/10.5045/br.2019.54.1.17

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