Egyptian Journal of Medical Human Genetics
 2018
DOI: 10.1016/j.ejmhg.2018.06.001
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Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion

Vesile Deniz Çelik
1
,
Betül Orhan Kiliç
2
,
Yasemin Ardıçoğlu Akışın
3
et al.
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