Cite
HARVARD Citation
Padmakumar, M. et al. (2019). A novel missense variant in SLC18A2 causes recessive brain monoamine vesicular transport disease and absent serotonin in platelets. JIMD reports. 47 (1), pp. 9-16. [Online].
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Padmakumar, M. et al. (2019). A novel missense variant in SLC18A2 causes recessive brain monoamine vesicular transport disease and absent serotonin in platelets. JIMD reports. 47 (1), pp. 9-16. [Online].