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JCI118492
JCI118492
http://dx.doi.org/10.1172/JCI118492
Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes
P356
Q24562650-9D57C346-3341-4791-A809-1E5A5DCB1666
P356
JCI118492
http://dx.doi.org/10.1172/JCI118492