Urinary glycerophosphoinositol is a potentially non-invasive clinically applicable biomarker for CLN3 disease

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Authors: Wendy Heywood, Ivan Doykov, Katy Vecchiato, Philippa B. Mills, Sara Mole, Paul Gissen
Cited by: 0

Fields of Study & Subjects

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

Publication details

Journal / source
Molecular Genetics and Metabolism
Volume
147
Issue
2
Pages
109463–109463
Publication date
1 February 2026
Language
EN