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Detection of a Major Lynch Syndrome-causing MLH1 Founder Variant in a Large-Scale Genotyped Cohort

Lauri J. Sipilä,Mervi Aavikko,Janne Ravantti,Samantha Martin,Teijo Kuopio,Laura Lahtinen, FinnGen,Päivi Peltomäki,Jukka-Pekka Mecklin,Lauri A. Aaltonen,Toni T. Seppälä

Familial Cancer（2024）

Cited 1|Views14
Key words
Lynch syndrome,Mismatch repair deficiency,Biobank,Genotype association,Personalized medicine
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