Evaluating Glc4 as a longitudinal marker of functional decline in late-onset Pompe disease

Molecular Genetics and Metabolism 2026

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Authors: Jordi Díaz‐Manera, Domenico Iannucci, James E. Clark, Cristina Domínguez‐González

DOI: 10.1016/j.ymgme.2025.109385

Cited by: 0

Fields of Study & Subjects

Lysosomal Storage Disorders Research Glycogen Storage Diseases and Myoclonus Biomedical Research and Pathophysiology