Genetic testing for haemochromatosis in patients with chondrocalcinosis.

Genetic testing for haemochromatosis in patients with chondrocalcinosis.

Hereditary haemochromatosis (HH) is the most common lethal monogenic human disease, affecting roughly 1 in 300 white northern Europeans. Homozygosity for the C282Y polymorphism within the HFE gene causes more than 80% of cases, with compound heterozygosity of the C282Y and H63D polymorphism also inc...

Bibliografske podrobnosti
Main Authors:	Timms, A, Sathananthan, R, Bradbury, L, Athanasou, N, Wordsworth, B, Brown, M
Format:	Journal article
Jezik:	English
Izdano:	2002

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