TARDBP mutation associated with semantic variant primary progressive aphasia, case report and review of the literature.

We describe a case of svPPA associated with MND in the same family, due to a mutation of the transactive response DNA binding protein (TARDBP) gene, and review the literature. PMID: 30773994 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/30773994?dopt=Abstract

Source: Neurocase - February 16, 2019 Category: Neurology Authors: González-Sánchez M, Puertas-Martín V, Esteban-Pérez J, García-Redondo A, Borrego-Hernández D, Méndez-Guerrero A, Llamas-Velasco S, Herrero-San Martín A, Cordero-Vázquez P, Herrero-Manso MC, Pérez-Martínez DA, Villarejo-Galende A Tags: Neurocase Source Type: research