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pro vyhledávání: '"Mehul Rathod"'
Publikováno v:
International Journal of Engineering Research and.
Publikováno v:
International Journal of Engineering Research and.
Autor:
S K, Sharma, Sangram, Mangudkar, Mehul, Rathod, Amrita, Verma, R L V, Phanikumar, Subodh, Garg, Ajinkya, Dhakne, Ramdas, Barure
Publikováno v:
The Journal of the Association of Physicians of India. 62(3)
Hereditary hemochromatosis (HH) is manifested as iron overload in different organs due to homozygosity of a single autosomal mutation. Two different mutations C282Y and H63D in the HFE gene have been associated with hereditary hemochromatosis cases.