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A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in ATP7B, SETX, SORL1, and FOXP1 Genes

Our aim was to analyze the phenotypic-genetic correlations in a patient diagnosed with early onset corticobasal syndrome with progressive non-fluent aphasia (CBS-PNFA), characterized by predominant apraxia of speech, accompanied by prominent right-sided upper-limb limb-kinetic apraxia, alien limb ph...

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Detalles Bibliográficos
Autores principales:	Gaweda-Walerych, Katarzyna, Sitek, Emilia J., Borczyk, Małgorzata, Narożańska, Ewa, Brockhuis, Bogna, Korostyński, Michał, Schinwelski, Michał, Siemiński, Mariusz, Sławek, Jarosław, Zekanowski, Cezary
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778325/ https://www.ncbi.nlm.nih.gov/pubmed/36553628 http://dx.doi.org/10.3390/genes13122361

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