Read + Share
Amedeo Smart
Independent Medical Education
Giugno A, Falcone E, Fortunato F, Sammarra I, et al. Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant. Eur J Neurol 2024;31:e16325.PMID: 38803061
Email
LinkedIn
Privacy Policy