Hemochromatosis is a disorder associated with iron overload. It is an autosomal recessive condition. It is caused by mutations in a gene called HFE. It is one of the most common human single gene disorders occurring in about 1 in 256 individuals of northern European descent. What then is the approximate carrier frequency of hemochromatosis in the northern European population?
A. 1 in 2
B. 1 in 8
C. 1 in 50
D. 1 in 100
E. 1 in 256
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