Longitudinal evaluation of olfactory function in individuals with Gaucher disease and GBA1 mutation carriers with and without Parkinson's disease

OBJECTIVE: Biallelic mutations in GBA1, which encodes the lysosomal enzyme glucocerebrosidase, cause the lysosomal storage disorder Gaucher disease (GD). In addition, mutations in GBA1 are the most common genetic risk factor for future development of Parkinson's disease (PD). However, most muta...

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Detalles Bibliográficos
Autores principales: Lopez, Grisel J., Lichtenberg, Jens, Tayebi, Nahid, Ryan, Emory, Lecker, Abigail L., Sidransky, Ellen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622935/
https://www.ncbi.nlm.nih.gov/pubmed/36330429
http://dx.doi.org/10.3389/fneur.2022.1039214

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