Associated Papers
Prime editing-installed suppressor tRNAs for disease-agnostic genome editing.
Pierce SE et al.
Nature, 2025
41261131 (PubMed )
Supplement: 41586_2025_9732_MOESM17_ESM.xlsx › Sequence_Context_Screen
A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report.
Bağrul İ et al.
Pediatric Rheumatology Online Journal, 2023
Pseudo-rheumatic manifestations of limping: Camptodactyly-arthropathy-coxa vara-pericarditis syndrome: Single case report and review of the literature.
Maniscalco V et al.
Frontiers in Pediatrics, 2022
Syndrome of progressive deforming non-inflammatory arthritis of childhood: two patients of camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Johnson N et al.
Rheumatology International, 2021
Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.
Yilmaz S et al.
Molecular Genetics & Genomic Medicine, 2018
29397575 (PubMed )
Supplement: MGG3-6-230-s002.xlsx › Appendix2
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