Detection of Rare and Unknown Mutations in ß- tathalassemia Traits in Iran

Beta-thalassemia, by its high frequency and heterogenecity, constitues a real problem of health in Iran. Aboute 13 beta globin mutations encompass 70-90% of mutations spectrum in Iran, the rest are rare or unknown. In this study six mutations of the codon IVSI-130(G-C), Fr16 (-C), codon35 (-C), fr23...

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Príomhchruthaitheoirí: M Habibi Roudknar (Údar), H Najmabadi (Údar), P Derakhshandeh (Údar), DD Farhud (Údar)
Formáid: LEABHAR
Foilsithe / Cruthaithe: Tehran University of Medical Sciences, 2003-07-01T00:00:00Z.
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