MLH1-associated leukemia
references
Mao G, Pan X, Gu L. Evidence that a mutation in the MLH1 3?-untranslated region confers a mutator phenotype and mismatch repair deficiency in patients with relapsed leukemia. J Biol Chem. 2008 Feb 8;283(6):3211-6. PMID: 18056700
Alotaibi H, Ricciardone MD, Ozturk M. Homozygosity at variant MLH1 can lead to secondary mutation in NF1, neurofibromatosis type I and early onset leukemia.Mutat Res. 2008 Jan 1;637(1-2):209-14. PMID: 17889038