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Do All Hemochromatosis Patients Have the Same Origin? A Pilot Study of Mitochondrial DNA and Y-DNA
Author(s) -
Caitlin Symonette,
Paul C. Adams
Publication year - 2011
Publication title -
canadian journal of gastroenterology
Language(s) - English
Resource type - Journals
eISSN - 1916-7237
pISSN - 0835-7900
DOI - 10.1155/2011/463810
Subject(s) - mitochondrial dna , haplotype , genetics , hereditary hemochromatosis , haplogroup , biology , hemochromatosis , human mitochondrial dna haplogroup , genetic analysis , sequence analysis , dna sequencing , genotype , dna , gene
Mitochondrial DNA (mtDNA) and Y-DNA analysis have been widely used to predict ancestral origin. Genetic anthropologists predict that human civilizations may have originated in central Africa one to two million years previously. Primary iron overload is not a common diagnosis among indigenous people of northern Africa, but hereditary hemochromatosis is present in approximately one in 200 people in northern Europe. MtDNA analysis has the potential to determine whether contemporary hemochromatosis patients have an ancient ancestral linkage.

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