Somatic GNAQ mutation in the forme fruste of Sturge-Weber syndrome

OBJECTIVE: To determine whether the GNAQ R183Q mutation is present in the forme fruste cases of Sturge-Weber syndrome (SWS) to establish a definitive molecular diagnosis. METHODS: We used sensitive droplet digital PCR (ddPCR) to detect and quantify the GNAQ mutation in tissues from epilepsy surgery...

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Detalles Bibliográficos
Autores principales: Hildebrand, Michael S., Harvey, A. Simon, Malone, Stephen, Damiano, John A., Do, Hongdo, Ye, Zimeng, McQuillan, Lara, Maixner, Wirginia, Kalnins, Renate, Nolan, Bernadette, Wood, Martin, Ozturk, Ezgi, Jones, Nigel C., Gillies, Greta, Pope, Kate, Lockhart, Paul J., Dobrovic, Alexander, Leventer, Richard J., Scheffer, Ingrid E., Berkovic, Samuel F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931068/
https://www.ncbi.nlm.nih.gov/pubmed/29725622
http://dx.doi.org/10.1212/NXG.0000000000000236

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931068/
https://www.ncbi.nlm.nih.gov/pubmed/29725622
http://dx.doi.org/10.1212/NXG.0000000000000236

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