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Frontiers | Functional Genomics of PRUNE1 in Neurodevelopmental Disorders (NDDs) Tied to Medulloblastoma (MB) and Other Tumors
An identical‐by‐descent novel splice‐donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families - Koko - 2021 - Annals of Human Genetics - Wiley Online Library
Papucs SCHOLL - Fiorilla F26699 1065 350 White - GLAMI.hu