A novel case of compound heterozygous GFPT1 congenital myasthenic syndrome with a coexisting heterozygous DYSF mutation: clinical and pathological insights

Neurological Sciences 2026

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Authors: Kamran Moradi, Leila Darki, Ryan W. Rebbe, Anna J. Mathew, Kyle M. Hurth, Said R. Beydoun

DOI: 10.1007/s10072-025-08642-5

Cited by: 0

References: 6

Fields of Study & Subjects

Myasthenia Gravis and Thymoma Muscle Physiology and Disorders Neurogenetic and Muscular Disorders Research

References 6