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A de novo DDX3X Variant Is Associated With Syndromic Intellectual Disability: Case Report and Literature Review

De novo DDX3X variants account for 1%–3% of intellectual disability (ID) in females and have been occasionally reported in males. Here, we report a female patient with severe ID and various other features, including epilepsy, movement disorders, behavior problems, sleep disturbance, precocious puber...

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Detalles Bibliográficos
Autores principales:	Chen, Yun, Liu, Kai-Yu, Yang, Zai-Lan, Li, Xiao-Huan, Xu, Rui, Zhou, Hao
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2020
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344189/ https://www.ncbi.nlm.nih.gov/pubmed/32714884 http://dx.doi.org/10.3389/fped.2020.00303

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