Associated Papers
Case Report: Clinical manifestations and treatment of two Chinese patients with FINCA syndrome carrying a novel variant of NHLRC2.
Liu Y et al.
Frontiers in Pediatrics, 2024
Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals.
Sczakiel HL et al.
European Journal of Human Genetics : Ejhg, 2023
Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease.
Tallgren A et al.
Frontiers in Neuroscience, 2023
FINCA syndrome-Defining neurobehavioral phenotype in survivors into late childhood.
Badura-Stronka M et al.
Molecular Genetics & Genomic Medicine, 2022
Select a paper to view details