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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Clin Lab Anal
Egile Nagusiak: Hashemi‐Soteh, Seyed Mohammad Bagher, Karami, Hossein, Mousavi, Seyed Saeid, Farazmandfar, Touraj, Tamadoni, Ahmad
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: John Wiley and Sons Inc. 2019
Gaiak:
Research Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6977355/
https://ncbi.nlm.nih.gov/pubmed/31478238
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.23018
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