Asymptomatic hemochromatosis case with HFE c.1007_47G>A, c.340+4T>C heterozygous mutations and alpha globin_3.7 kb deletion
By: Celik, Vesile Deniz; Kilic, Betul Orhan; Akar, Najat…[et al.]. The Egyptian Journal of Medical Human Genetics. Vol. 19, no. 4 (Oct. 2018), pp.433-435, 3 p.
Subjects: Hemochromatosis