Associated Papers
Exploring the Impact of RNU4-2 Defects on Neurodevelopmental Disorders in a Korean Population.
Hong J et al.
Clinical Genetics, 2026
Mutations in the U4 snRNA gene RNU4-2 cause one of the most prevalent monogenic neurodevelopmental disorders.
Greene D et al.
Nature Medicine, 2024
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders.
Chen Y et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
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