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pro vyhledávání: '"Faïza Zbidi"'
Autor:
Najla Soyah, Abdelbasset Amara, Faïza Zbidi, Ilhem Charfeddine, Abdelkarim Ayedi, Ahlem M'sakni, Saoussen Abroug, Jihene Bouguila, Hechmi Ben Hamouda, Adnène Mlika, Khalid Hlel, Taheni Ben Lazreg, Ali Saad, N. Zouari, Anouar Chaieb, Lamia Boughamoura, Moez Gribaa
Publikováno v:
Hemoglobin. 39:251-255
The β hemoglobinopathies [β-thalassemia (β-thal) and structural hemoglobin (Hb) variants such as Hb S (HBB: c.20A T) and Hb E (HBB: c.79G A)] are among the most common inherited diseases worldwide. In Tunisia, due to the high prevalence of consang