Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity.

Authors Parsons MT, Whiley PJ, Beesley J, et al.
Citation Mol Carcinog. 2015 Jul;54(7):513-22.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24302565/
PMCID PMC4041856