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Creutzfeldt–Jakob disease in a heterozygous GBA mutation carrier: Coincidence or consequence?
Enfermedad de Creutzfeldt-Jakob en un portador heterocigoto de una mutación del gen GBA: ¿coincidencia o consecuencia?
I.V. Carvalhoa,
Corresponding author
inesvideiradecarvalho@gmail.com

Corresponding author.
, D. Damasa, I. Baldeirasb,c, M.R. Almeidab, H. Gensa, G.C. Santoa
a Neurology Department, Centro Hospitalar e Universitário de Coimbra Praceta Professor Mota Pinto, Coimbra, Portugal
b Center for Neuroscience and Cell Biology, University of Coimbra, Portugal
c Faculty of Medicine, University of Coimbra, Portugal

Article

This article is available in English

Creutzfeldt–Jakob disease in a heterozygous GBA mutation carrier: Coincidence or consequence?

I.V. Carvalho, D. Damas, I. Baldeiras, M.R. Almeida, H. Gens, G.C. Santo
10.1016/j.nrleng.2024.07.005
Neurologia. 2024;39:614-6
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