Molecular patterns of β-thalassemia mutations of Saudi patients referred to King Faisal Specialist Hospital and Research Center
Background: Beta thalassemias are a group of hereditary blood disorders that are characterized by reduction or complete absence of the β-globin chain synthesis due to mutations, affecting critical areas of the β-globin gene on the chromosome 11. The disease is inherited in an autosomal recessive man...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Wolters Kluwer Medknow Publications
2017-01-01
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| سلاسل: | Journal of Applied Hematology |
| الموضوعات: | |
| الوصول للمادة أونلاين: | http://www.jahjournal.org/article.asp?issn=1658-5127;year=2017;volume=8;issue=3;spage=99;epage=104;aulast=Mashi |
| الوسوم: |
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