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Oncoimmunology (2019) 8(9):e1624129
A highly relevant 2017 double-blind trial by Withee et al
Mutations in DDHD2, encoding an intracellular phospholipase A1, cause a recessive form of complex hereditary spastic paraplegia
By setting up different culture plates with varying concentrations of the blend, you could map out a full dose-response curve
