Neuropathological alterations in TPP1-deficient cynomolgus macaques recapitulate key features of human CLN2 disease

Molecular Genetics and Metabolism 2026

View at publisher

Authors: Ewa Ziółkowska, Sophie H. Wang, Grace Robinson Kick, Keigo Takahashi, Jonathan D. Cooper

DOI: 10.1016/j.ymgme.2025.109684

Cited by: 0

Fields of Study & Subjects

Lysosomal Storage Disorders Research Glycogen Storage Diseases and Myoclonus Metabolism and Genetic Disorders