Novel CAPN1 missense variants in complex hereditary spastic paraplegia with early‐onset psychosis

CAPN1‐associated hereditary spastic paraplegia (SPG76) is a rare and clinically heterogenous syndrome due to loss of calpain‐1 function. Here we illustrate a translational approach to the case of an 18‐year‐old patient who first presented with psychiatric symptoms followed by spastic gait, intention...

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Detalles Bibliográficos
Autores principales: Alecu, Julian E., Saffari, Afshin, Jumo, Hellen, Ziegler, Marvin, Strelko, Oleksandr, Brownstein, Catherine A., Gonzalez‐Heydrich, Joseph, Rodan, Lance H., Gorman, Mark P., Sahin, Mustafa, Ebrahimi‐Fakhari, Darius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Brief Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994985/
https://www.ncbi.nlm.nih.gov/pubmed/35297214
http://dx.doi.org/10.1002/acn3.51531

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994985/
https://www.ncbi.nlm.nih.gov/pubmed/35297214
http://dx.doi.org/10.1002/acn3.51531

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