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...
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| Principais autores: | , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Wolters Kluwer Medknow Publications
2017-01-01
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| Serier: | Journal of Applied Hematology |
| Fag: | |
| Online adgang: | http://www.jahjournal.org/article.asp?issn=1658-5127;year=2017;volume=8;issue=3;spage=99;epage=104;aulast=Mashi |
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