Loss of PHF6 leads to aberrant development of human neuron-like cells

Pathogenic variants in PHD finger protein 6 (PHF6) cause Borjeson–Forssman–Lehmann syndrome (BFLS), a rare X-linked neurodevelopmental disorder, which manifests variably in both males and females. To investigate the mechanisms behind overlapping but distinct clinical aspects between genders, we asse...

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Detalles Bibliográficos
Autores principales: Fliedner, Anna, Gregor, Anne, Ferrazzi, Fulvia, Ekici, Arif B., Sticht, Heinrich, Zweier, Christiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642390/
https://www.ncbi.nlm.nih.gov/pubmed/33149206
http://dx.doi.org/10.1038/s41598-020-75999-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642390/
https://www.ncbi.nlm.nih.gov/pubmed/33149206
http://dx.doi.org/10.1038/s41598-020-75999-2

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