A syndrome featuring developmental disorder of the nervous system induced by a novel mutation in the TCF20 gene, rarely concurrent immune disorders: a case report

Background: The expression of TCF20 is the most widespread in brain tissue. TCF20 depletion or mutation can affect the proliferation and differentiation of embryonic neurons, leading to developmental disorder of the central nervous system and subsequent rare syndrome featuring. Case presentation: He...

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Detalles Bibliográficos
Autores principales: Huang, Si, Xu, Jiaxin, Li, Yiyang, Mo, Wenhui, Lin, Xiuwen, Wang, Yajun, Liang, Fujian, Bai, Yan, Huang, Guochun, Chen, Jing, Xin, Jing, Ma, Guoda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248432/
https://www.ncbi.nlm.nih.gov/pubmed/37303953
http://dx.doi.org/10.3389/fgene.2023.1192668

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248432/
https://www.ncbi.nlm.nih.gov/pubmed/37303953
http://dx.doi.org/10.3389/fgene.2023.1192668

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