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APA Citation
Maselli, R. A., van der Linden, H., & Ferns, M. (2020). recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly conserved C‐terminal amino acid sequence. American journal of medical genetics, 182(7), 1744–1749. http://access.bl.uk/ark:/81055/vdc_100103759536.0x00000b