Associated Papers
Expanding the phenotype of UPF3B-related disorder: Case reports and literature review.
Romano F et al.
American Journal of Medical Genetics. Part A, 2024
Functional roles of human Up-frameshift suppressor 3 (UPF3) proteins: From nonsense-mediated mRNA decay to neurodevelopmental disorders.
Deka B et al.
Biochimie, 2021
Broadening the phenotype associated with mutations in UPF3B: two further cases with renal dysplasia and variable developmental delay.
Lynch SA et al.
European Journal of Medical Genetics, 0
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