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Novel GRN Mutations in Patients with Corticobasal Syndrome

Loss-of-function GRN mutations lead to GRN haploinsufficiency and consequently neurodegeneration with significant heterogeneity in clinical presentation of various syndromes. The aim of this study was to investigate the genetics and clinical features of patients with GRN-related frontotemporal lobar...

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Detalles Bibliográficos
Autores principales:	Taghdiri, Foad, Sato, Christine, Ghani, Mahdi, Moreno, Danielle, Rogaeva, Ekaterina, Tartaglia, Maria Carmela
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group 2016
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785496/ https://www.ncbi.nlm.nih.gov/pubmed/26961809 http://dx.doi.org/10.1038/srep22913

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