Batten Disease (CLN3): A High-Unmet-Need Rare Neurodegenerative Disorder Driving Early Drug Discovery Investment CLN3, or Batten disease, is a rare childhood-onset neurodegenerative disorder caused by a ~1 kb deletion in the CLN3 gene, precisely on exons 7 and 8 on chromosome 16p11.2., predicted to result in a truncated protein. It is the most common subtype […]