Alpha‐globin gene mutation spectrum in patients with microcytic hypochromic anemia from Mazandaran Province, Iran

BACKGROUND: It is estimated about 7% of the world population is carriers of hemoglobin diseases. Alpha‐thalassemia is one of the most common hereditary hemoglobin disorders in the world. This study investigated alpha‐globin mutations in potential carriers with hypochromic and microcytic anemia from...

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Detalles Bibliográficos
Autores principales: Hashemi‐Soteh, Seyed Mohammad Bagher, Karami, Hossein, Mousavi, Seyed Saeid, Farazmandfar, Touraj, Tamadoni, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977355/
https://www.ncbi.nlm.nih.gov/pubmed/31478238
http://dx.doi.org/10.1002/jcla.23018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977355/
https://www.ncbi.nlm.nih.gov/pubmed/31478238
http://dx.doi.org/10.1002/jcla.23018

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