Associated Papers
Unraveling the Diversity of RANBP2: Protein Isoforms and Implications for Cellular Function and Human Disease.
Desgraupes S et al.
Journal of Molecular Biology, 2025
Clinical and genetic characteristics of RANBP2 mutations in children with acute necrotizing encephalopathy.
Fan C et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2025
De novo RANBP2 variant in a fetal demise case with cerebral intraparenchymal hemorrhage.
Meroni A et al.
American Journal of Medical Genetics. Part A, 2023
A novel variation in RANBP2 associated with infection-triggered familial acute necrotizing encephalopathy.
Hu Y et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2022
Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation.
Sell K et al.
Brain & Development, 2016
Acute Necrotizing Encephalopathy: 2 Case Reports on RANBP2 Mutation.
Hartley M et al.
Child Neurology Open, 0
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