[Combinations of genotypes according to polymorphous systems of CYP1A1, GSTM1 and Nat2 were detected, which is typical of IDA patients and which can be used as molecular-genetic markers of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE