Successful treatment of a Fabry patient with pegunigalsidase alfa after developing angioedema and anaphylactic shock on agalsidase alfa alpha and beta

Molecular Genetics and Metabolism 2026

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Authors: Gheona Altarescu

DOI: 10.1016/j.ymgme.2025.109308

Cited by: 0

Fields of Study & Subjects

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