Heterozygous FOXJ1 Mutations Cause Incomplete Ependymal Cell Differentiation and Communicating Hydrocephalus

Heterozygous mutations affecting FOXJ1, a transcription factor governing multiciliated cell development, have been associated with obstructive hydrocephalus in humans. However, factors that disrupt multiciliated ependymal cell function often cause communicating hydrocephalus, raising questions about...

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Detalles Bibliográficos
Autores principales: Hou, Connie C., Li, Danielle, Berry, Bethany C., Zheng, Shaokuan, Carroll, Rona S., Johnson, Mark D., Yang, Hong Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661798/
https://www.ncbi.nlm.nih.gov/pubmed/37620636
http://dx.doi.org/10.1007/s10571-023-01398-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661798/
https://www.ncbi.nlm.nih.gov/pubmed/37620636
http://dx.doi.org/10.1007/s10571-023-01398-6

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