Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion
Çelik, Vesile Deniz, Kiliç, Betul Orhan, Akişin, Yasemin Ardiçoğlu, Tükün, Fatma Ajlan, Akar, NejatVolume:
19
Language:
english
Journal:
Egyptian Journal of Medical Human Genetics
DOI:
10.1016/j.ejmhg.2018.06.001
Date:
October, 2018
File:
PDF, 935 KB
english, 2018