729-43-1

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Status of HFE mutation in thalassemia syndromes in north India.

Sarita Agarwal et al.

Annals of hematology, 86(7), 483-485 (2007-04-03)

Hereditary hemochromatosis is an autosomal recessive and most commonly inherited single gene disorder among Caucasians, with a prevalence of 5 per 1,000 and a carrier frequency of 1 in 10. Two point mutations were described and are referred as C282Y

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