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Catherine, I wasn't told which gene is involved in the drug trial but I did see (upside down and in bad doctor handwriting) what looked like HFE c282y. I looked it up and it seems to be a haemachromatosis gene mutation.
Hope this helps.
Regards
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Copper deficiency bone marrow failure (MDS RAEB 1), neuromyelopathy.
FISH reported normal cytogenetics but gene testing showed
Xq 8.21 mutation
Xq19.36 mutation
Xq21.40. mutation
1p36. Mutation
15q11.2 deletion
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