A Unique Genetic Duality: GAK and SCN4A Mutations in Myasthenic Syndrome and Early-Onset Parkinsonism in a Peruvian Woman: A Case Report

Authors
Category Primary study
Conference2025 International Congress of Parkinson's Disease and Movement Disorders
Year 2025
This article has no abstract
Epistemonikos ID: 574aebb0bd2a1df514ef2c0566ad1fa241d4990d
First added on: Nov 18, 2025