Associated Papers
Genetic Burden in Congenital Anomalies of the Mitral and Tricuspid Valves: A Case-Control Study.
Campos-Garcia FJ et al.
Pediatric Cardiology, 2026
Essential role of NONO-HOXA1-Wnt axis in cardiomyocyte differentiation.
Feng Z et al.
Nature Communications, 2026
Case Report: A female case of X-linked intellectual disability syndrome type 34 caused by a NONO frameshift variant and literature review.
Zhang Y et al.
Frontiers in Pediatrics, 2026
Genetic Burden in Congenital Anomalies of the Mitral and Tricuspid Valves: A Case-Control Study.
Campos-Garcia FJ et al.
Pediatric Cardiology, 2025
NONO-related X-linked intellectual disability syndrome: Further clinical and molecular delineation.
Planté-Bordeneuve P et al.
European Journal of Medical Genetics, 2025
X-linked intellectual developmental disorder with onset of neonatal heart failure: A case report and literature review.
Xi H et al.
Molecular Genetics and Metabolism Reports, 2024
Genetic and phenotypic spectrum in the NONO-associated syndromic disorder.
Roessler F et al.
American Journal of Medical Genetics. Part A, 2023
Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation.
Lin Y et al.
Orphanet Journal of Rare Diseases, 2021
Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONO.
Sewani M et al.
American Journal of Medical Genetics. Part A, 2020
Case Report: Characterization of a Novel NONO Intronic Mutation in a Fetus With X-Linked Syndromic Mental Retardation-34.
Sun H et al.
Frontiers in Genetics, 2020
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