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MOLECULAR BASIS OF BETA THALASSEMIA MUTATIONS IN EGYPTIAN PATIENTS

Thalassemia is a wide range hereditary disease with high incidence in Egypt along with the high frequency of consanguineous marriages. Investigation the heterogeneity, molecular basis, and natural history are the most effective methods to deal with the thalassemia to develop effective method for man...

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Detaylı Bibliyografya
Asıl Yazarlar: Khalil Elhalfawy, Ahmed Daif, Osama Shalaan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: University of Sadat City, Genetic Engineering & Biotechnology Research Institute (GEBRI) 2017-06-01
Seri Bilgileri:Research Journal of Applied Biotechnology
Konular:
Online Erişim:https://rjab.journals.ekb.eg/article_57658_ae22ee8493d48a33ac061b1382dd9ce6.pdf
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