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Heterozygous SPTLC1 p.Leu39del is a major cause of slow-progressing juvenile ALS
Language
EN
Article de revue
This item was published in
Journal of Neurology, Neurosurgery and Psychiatry. 2024-02-14, vol. 95, n° 3, p. 288-290
English Keywords
Humans
Amyotrophic Lateral Sclerosis
Mutation
Serine C-Palmitoyltransferase