A de novo c.113 T   >  C: p.L38R mutation of SPTLC1: case report of a girl with sporadic juvenile amyotrophic lateral sclerosis

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Source: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration - October 7, 2022 Category: Neurology Authors: Xiaoxuan Liu Ji He Weiyi Yu Dongsheng Fan Source Type: research