Expansion of Clinical and Genetic Spectrum of DDX3X Neurodevelopmental Disorder in 23 Chinese Patients

AIM: De novo DDX3X variants account for 1–3% of unexplained intellectual disability cases in females and very rarely in males. Yet, the clinical and genetic features of DDX3X neurodevelopmental disorder in the Chinese cohort have not been characterized. METHOD: A total of 23 Chinese patients (i.e.,...

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Detalles Bibliográficos
Autores principales: Dai, Yuwei, Yang, Zhuanyi, Guo, Jialing, Li, Haoyu, Gong, Jiaoe, Xie, Yuanyuan, Xiao, Bo, Wang, Hua, Long, Lili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981727/
https://www.ncbi.nlm.nih.gov/pubmed/35392274
http://dx.doi.org/10.3389/fnmol.2022.793001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981727/
https://www.ncbi.nlm.nih.gov/pubmed/35392274
http://dx.doi.org/10.3389/fnmol.2022.793001

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