The parent and family impact of CLN3 disease: an observational survey-based study

CLN3 disease (also known as CLN3 Batten disease or Juvenile Neuronal Ceroid Lipofuscinosis) is a rare pediatric neurodegenerative disorder caused by biallelic mutations in CLN3. While extensive efforts have been ...

Source: Orphanet Journal of Rare Diseases - March 18, 2024 Category: Internal Medicine Authors: Angela Schulz, Nita Patel, Jon J. Brudvig, Frank Stehr, Jill M. Weimer and Erika F. Augustine Tags: Research Source Type: research