Early manifestations, treatment outcome data, family impact, and emerging therapies necessitates newborn screening for Fabry disease

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Authors: Rachelen S. Varghese, Dawn A. Laney, Brian E. Jones
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
109652–109652
Publication date
1 February 2026
Language
EN