Associated Papers
Phase separation as a possible mechanism for dosage sensitivity.
Yang L et al.
Genome Biology, 2024
38225666 (PubMed )
Supplement: 13059_2023_3128_MOESM3_ESM.xlsx › NMD-escaping_mutations
A new variant of MYCN gene as a cause of Feingold syndrome.
Zeka N et al.
Clinical Case Reports, 2022
Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype.
Tedesco MG et al.
American Journal of Medical Genetics. Part A, 2021
Select a paper to view details