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Alpha thalassemia deletions found in suspected cases of beta thalassemia major in Pakistani population
BACKGROUND & OBJECTIVE: Alpha (α) thalassemia is a hereditary disorder and is caused by deletions or mutations in globin genes. It is present in two clinically significant forms: hemoglobin Bart hydrops fetalis (Hb Bart) syndrome and hemoglobin H (HbH) disease. It is highly prevalent in South-Ea...
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| Publicado no: | Pak J Med Sci |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Professional Medical Publications
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5432714/ https://ncbi.nlm.nih.gov/pubmed/28523047 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12669/pjms.332.11834 |
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