Deniz: The electronic database for ß-thalassemia mutations in the Arab world
نویسنده
چکیده
aid in the analysis of data, and (c) the interpretation of results in a biomedically meaningful manner.1 To fulfill these aims, vast amounts of information are stored in information repositories called databases. Database types differ considerably depending, primarily, on the nature of the information stored. In biomedical applications, the hierarchical and relational schemes are widely used. A relational database stores data in 2-dimensional tables that embody different Deniz: The electronic database for ß-thalassemia mutations in the Arab world
منابع مشابه
بررسی مولکولی جهش های غیر حذفی ژن های آلفاگلوبین بیماران آلفا تالاسمی دراستان کرمانشاه
Background: Alpha thalassemia is a single gene disorder, inherited in an autosomal recessive manner. The thalassemia occurs mostly in peoples from the Mediterranean to Southeast Asia. The present study was aimed to identify the prevalence of nondeletional Alpha thalassemia mutations in our samples in the Kermanshah province. Methods : This study included Alpha thalassemia individuals who ha...
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The Arab countries encompass a wide region stretching from the Persian Gulf to the Atlantic Ocean. The Arab population is quite heterogeneous and has experienced various invasions and migrations throughout history. beta-thalassemia is endemic in all countries of the Arab world. Our review of the molecular basis of beta-thalassemia in various Arab countries reveals the presence of 52 mutations, ...
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Background and purpose : bata thlassemia is the most common monogenic disorders in Iran. The gene frequency varies the country. Sistan and Baluchistan province, located in the southeast of iran with more than 1200 affected individuals, represents one of the regions where thalassemia id not only an important public health problem but also a socioeconomic problem. As a matter of fact high frequ...
متن کاملMolecular 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 hemoglobinopathies in Iran, α-thal carriers have come to more attention. Therefore, the fr...
متن کاملفراوانی موتاسیونهای ژن بتا - گلوبین در بیماران بتا-تالاسمی شرق مازندران
Background and purpose: Beta-thalassemia is the most common inherited disorder in the world, especially in Iran. According to Iranian thalassemia society registry, 18616 thalassemia patients now living in Iran, which Mazandaran and Fars provinces have the most patients. Previous reports have shown that the frequency of b-thalassemia carriers is more than 10% in Mazandaran province. Although b...
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تاریخ انتشار 2003