Yüklüyor......
Molecular Basis of α-Thalassemia in Iran
Alpha-thalassemia (α-thal) is probably the most prevalent monogenic condition in the world. Deletions are the most common types of mutations in α-thal, followed by point mutations and small insertion/deletion. In the context of national screening program for prevention of thalassemia and hemoglobino...
Kaydedildi:
| Yayımlandı: | Iran Biomed J |
|---|---|
| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Pasteur Institute
2018
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5712386/ https://ncbi.nlm.nih.gov/pubmed/29115104 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22034/ibj.22.1.6 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|