Novel congenital myasthenic syndrome caused by homozygous mutation in 3′-UTR of low-density lipoprotein receptor-related protein 6 (LRP6) gene (P7-13.010)
Neurology | December 6, 2023 | Volume: 98 | Issue: 18_supplement | Pages: No page available
10.1212/wnl.98.18_supplement.1796