Functional analysis of rare variants in mismatch repair proteins augments results from computation-based predictive methods
Author:
Affiliation:
1. Molecular Therapeutics Program, Fox Chase Cancer Center, Philadelphia, PA, USA
2. Immersion Science Program, Fox Chase Cancer Center, Philadelphia, PA, USA
3. Department of Clinical Genetics, Fox Chase Cancer Center, Philadelphia, PA, USA
Publisher
Informa UK Limited
Subject
Cancer Research,Pharmacology,Oncology,Molecular Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/15384047.2017.1326439
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1. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
2. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
3. Milestones of Lynch syndrome: 1895–2015
4. Functional characterization ofMLH1missense variants identified in lynch syndrome patients
5. Endonucleolytic Function of MutLα in Human Mismatch Repair
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