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Case Report: Clinical Features of a Chinese Boy With Epileptic Seizures and Intellectual Disabilities Who Carries a Truncated NUS1 Variant
The mental retardation-55 with seizures (MRD55) is a rare genetic disease characterized by developmental delay, intellectual disability, language delay and multiple types of epileptic seizures. It is caused by pathogenic variants of the NUS1 gene, which encodes Nogo-B receptor (NgBR), a necessary su...
Autores principales: | Zhang, Pingli, Cui, Di, Liao, Peiyuan, Yuan, Xiang, Yang, Nuan, Zhen, Yuanyuan, Yang, Jing, Huang, Qikun |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438189/ https://www.ncbi.nlm.nih.gov/pubmed/34532305 http://dx.doi.org/10.3389/fped.2021.725231 |
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