Different Types of Complications in Patients Suffering from B-Thalassemia (Thalassemia Major)
INTRODUCTION Thalassemia is a heterogeneous group of gene disorders caused byan inherited mutation or deletion of genes at chromosome 16 & 11 resulting in decreased synthesis of adult hemoglobin. Its incidence is higher in people/children having a positive family history of Thalassemia Among its va...
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| Principais autores: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Gandhara University
2017-09-01
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| coleção: | Journal of Gandhara Medical and Dental Sciences |
| Assuntos: | |
| Acesso em linha: | http://jgmds.org.pk/index.php/JGMDS/article/view/30 |
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