Associated Papers
Prime editing optimized RTT permits the correction of the c.8713C>T mutation in DMD gene.
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Molecular Therapy. Nucleic Acids, 2022
Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk.
Jia X et al.
American Journal of Human Genetics, 2021
33357406 (PubMed )
Supplement: mmc2.xlsx › TableS5_AllVariants
Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma.
Abdel-Rahman MH et al.
Ophthalmology, 2020
Splice site mutations in mismatch repair genes and risk of cancer in the general population.
Thomsen M et al.
Familial Cancer, 2013
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