Molecular analysis of hemoglobinopathies in a large ethnic Hakka population in southern China

Thalassemia is an inherited autosomal recessive disorder with microcytic hypochromic anemia resulting from reduced or absent synthesis of 1 or more of the globin chains of hemoglobin. This study provided the insight into prevalence and molecular characterization of thalassemia in Hakka population. 1...

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Detalles Bibliográficos
Autores principales: Zhao, Pingsen, Wu, Heming, Weng, Ruiqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250515/
https://www.ncbi.nlm.nih.gov/pubmed/30407298
http://dx.doi.org/10.1097/MD.0000000000013034

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250515/
https://www.ncbi.nlm.nih.gov/pubmed/30407298
http://dx.doi.org/10.1097/MD.0000000000013034

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