Alternating hemiplegia of childhood: evolution over time and mouse model corroboration

Alternating hemiplegia of childhood is a rare neurodevelopmental disorder caused by ATP1A3 mutations. Some evidence for disease progression exists, but there are few systematic analyses. Here, we evaluate alternating hemiplegia of childhood progression in humans and in the D801N knock-in alternating...

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Detalles Bibliográficos
Autores principales: Uchitel, Julie, Wallace, Keri, Tran, Linh, Abrahamsen, Tavis, Hunanyan, Arsen, Prange, Lyndsey, Jasien, Joan, Caligiuri, Laura, Pratt, Milton, Rikard, Blaire, Fons, Carmen, De Grandis, Elisa, Vezyroglou, Aikaterini, Heinzen, Erin L, Goldstein, David B, Vavassori, Rosaria, Papadopoulou, Maria T, Cocco, Isabella, Moré, Rebecca, Arzimanoglou, Alexis, Panagiotakaki, Eleni, Mikati, Mohamad A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361420/
https://www.ncbi.nlm.nih.gov/pubmed/34396101
http://dx.doi.org/10.1093/braincomms/fcab128

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361420/
https://www.ncbi.nlm.nih.gov/pubmed/34396101
http://dx.doi.org/10.1093/braincomms/fcab128

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