Psychosis in NUS1 de novo mutation: New phenotypical presentation
Author:
Affiliation:
1. Hospital Universitario Onofre Lopes Universidade Federal do Rio Grande do Norte Natal Brazil
2. National Institute of Science and Technology in Translational Medicine University of Sao Paulo Sao Paulo Brazil
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13867
Reference5 articles.
1. NUS1 mutation in a family with epilepsy, cerebellar ataxia, and tremor
2. Recurrent NUS1 canonical splice donor site mutation in two unrelated individuals with epilepsy, myoclonus, ataxia and scoliosis - a case report
3. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
4. Genetic analysis of NUS1 in Chinese patients with Parkinson's disease
5. Coding mutations inNUS1contribute to Parkinson’s disease
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