GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome

OBJECTIVE: To describe better the motor phenotype, molecular genetic features, and clinical course of GNAO1-related disease. METHODS: We reviewed clinical information, video recordings, and neuroimaging of a newly identified cohort of 7 patients with de novo missense and splice site GNAO1 mutations,...

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Detalles Bibliográficos
Autores principales: Danti, Federica Rachele, Galosi, Serena, Romani, Marta, Montomoli, Martino, Carss, Keren J., Raymond, F. Lucy, Parrini, Elena, Bianchini, Claudia, McShane, Tony, Dale, Russell C., Mohammad, Shekeeb S., Shah, Ubaid, Mahant, Neil, Ng, Joanne, McTague, Amy, Samanta, Rajib, Vadlamani, Gayatri, Valente, Enza Maria, Leuzzi, Vincenzo, Kurian, Manju A., Guerrini, Renzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362187/
https://www.ncbi.nlm.nih.gov/pubmed/28357411
http://dx.doi.org/10.1212/NXG.0000000000000143

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362187/
https://www.ncbi.nlm.nih.gov/pubmed/28357411
http://dx.doi.org/10.1212/NXG.0000000000000143

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