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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...
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| Publicado no: | Iran Biomed J |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Pasteur Institute
2018
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| Assuntos: | |
| Acesso em linha: | 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 |
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