YWHAZ variation causes intellectual disability and global developmental delay with brain malformation

YWHAZ encodes an adapter protein 14–3-3ζ, which is involved in many signaling pathways that control cellular proliferation, migration and differentiation. It has not been definitely correlated to any phenotype in OMIM. To investigate the role of YWHAZ gene in intellectual disability and global devel...

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Detalles Bibliográficos
Autores principales: Wan, Rui-Ping, Liu, Zhi-Gang, Huang, Xiao-Fei, Kwan, Ping, Li, Ya-Ping, Qu, Xiao-Chong, Ye, Xing-Guang, Chen, Feng-Ying, Zhang, Da-Wei, He, Ming-Feng, Wang, Jie, Mao, Yu-Ling, Qiao, Jing-Da
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851741/
https://www.ncbi.nlm.nih.gov/pubmed/36001342
http://dx.doi.org/10.1093/hmg/ddac210

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851741/
https://www.ncbi.nlm.nih.gov/pubmed/36001342
http://dx.doi.org/10.1093/hmg/ddac210

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