Search Results - "Dhillon, Barjinderjit Kaur"

Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India by Dhillon, Barjinderjit Kaur, Das, Reena, Garewal, Gurjeewan, Chawla, Yogesh, Dhiman, R K, Das, Ashim, Duseja, Ajay, Chandak, G R

“…To identify the frequency of iron overload and study the three mutations in the HFE gene (C282Y, H63D, and S65C) in patients with chronic liver disorders (CLD)…”
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Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians by Dhillon, Barjinderjit Kaur, Chopra, Gunjan, Jamwal, Manu, Chandak, Giri Raj, Duseja, Ajay, Malhotra, Pankaj, Chawla, Yogesh Kumar, Garewal, Gurjeewan, Das, Reena

“…Hereditary hemochromatosis (HH) is a rare disorder in Indians and is not associated with the common mutation Cys282Tyr in HFE gene found in Caucasians. Non-HFE…”
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H63D mutation in HFE gene is common in Indians and is associated with the European haplotype by DHILLON, BARJINDERJIT KAUR, PRAKASH, SWAMI, CHANDAK, G. R., CHAWLA, Y. K., DAS, REENA

“…The common C282Y mutation (HFE gene) in hereditary hemochromatosis patients of European origin is absent in Indians. The frequency of the second common…”
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