Associated Papers
Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism.
Dafsari HS et al.
Annals of Neurology, 2025
41053928 (PubMed )
Supplement: ANA-98-932-s004.xlsx › PATIENTS
Clinical Presentation and Molecular Characterization of 3 Patients with Vici Syndrome: Two Novel Variants in the EPG5 Gene.
Selamioğlu A et al.
Molecular Syndromology, 2024
The first Chinese case of Vici syndrome with novel compound heterozygous sequence variants in EPG5.
Dong L et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience, 2021
Two cases of Vici syndrome presenting with corpus callosum agenesis, albinism, and severe developmental delay.
Hızal M et al.
The Turkish Journal of Pediatrics, 2020
EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy.
Byrne S et al.
Brain : a Journal of Neurology, 2016
Vici syndrome in siblings born to consanguineous parents.
Tasdemir S et al.
American Journal of Medical Genetics. Part A, 2016
First description of a patient with Vici syndrome due to a mutation affecting the penultimate exon of EPG5 and review of the literature.
Ehmke N et al.
American Journal of Medical Genetics. Part A, 2014
Familial corpus callosum agenesis.
Ozdirim E et al.
The Turkish Journal of Pediatrics, 0
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