https://www.news-medical.net/news/20200228/Research-reveals-key-role-of-a-protein-in-rare-Batten-disease.aspx
Research reveals key role of a protein in rare Batten disease
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Reviewed by James Ives, M.Psych. (Editor)Feb 28 2020
Professor Stéphane Lefrançois, a researcher at the Institut National de la Recherche Scientifique (INRS), is working on Batten disease, a neurodegenerative genetic disease that primarily affects children. His research focuses on the most common form of the disease – Batten CLN 3 – which is caused by mutations in the protein of the same name and for which there is still no cure.
CLN3
