Deficiency of the Lysosomal Protein CLN5 Alters Lysosomal Function and Movement

Batten disease is a devastating, childhood, rare neurodegenerative disease characterised by the rapid deterioration of cognition and movement, leading to death within ten to thirty years of age. One of the thirteen Batten disease forms, CLN5 Batten disease, is caused by mutations in the CLN5 gene, l...

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Detalles Bibliográficos
Autores principales: Basak, Indranil, Hansen, Rachel A., Ward, Michael E., Hughes, Stephanie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533494/
https://www.ncbi.nlm.nih.gov/pubmed/34680045
http://dx.doi.org/10.3390/biom11101412

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533494/
https://www.ncbi.nlm.nih.gov/pubmed/34680045
http://dx.doi.org/10.3390/biom11101412

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