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Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis.
Rhodes, D A, Raha-Chowdhury, R, Cox, T M, Trowsdale, JVolume:
34
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.34.9.761
Date:
September, 1997
File:
PDF, 852 KB
english, 1997