Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype

ConclusionOur study suggests that in HSP patients with psychiatric symptoms,ATP13A2 mutations should be suspected, especially if they also have extrapyramidal symptoms.

https://onlinelibrary.wiley.com/doi/abs/10.1002/mgg3.1052?af=R

Source: Molecular Genetics & Genomic Medicine - January 14, 2020 Category: Genetics & Stem Cells Authors: Mehrdad A. Estiar, Etienne Leveille, Dan Spiegelman, Nicolas Dupre, Jean-Fran çois Trempe, Guy A. Rouleau, Ziv Gan‐Or Tags: ORIGINAL ARTICLE Source Type: research