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APA Citation
Padmakumar, M., Jaeken, J., Ramaekers, V., Lagae, L., Greene, D., Thys, C., Van Geet, C., BioResource, N., Stirrups, K., Downes, K., Turro, E., & Freson, K. (2019). a novel missense variant in SLC18A2 causes recessive brain monoamine vesicular transport disease and absent serotonin in platelets. JIMD reports, 47(1), 9–16. http://access.bl.uk/ark:/81055/vdc_100081456429.0x000004