Method and probes for genetic diagnosis of hemochromatosis.

摘要

Probe for the diagnosis of hemochromatosis, characterized in that the probe is capable of hybridizing with nucleic acids of a biological sample in a region corresponding to a region of the cDNA sequence of the HFE gene containing nucleotide 502 to determine if a G- T mutation at position 502 of the cDNA sequence of the HFE gene.