Browse result page of "Disorder" of RareLSD

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ID1047ENZYMEL-Aminoacid oxidaseGENEIL4I1EC NUMBER1.4.3.2FAMILYFlavin monoamine oxidaseCYTOGENETICS19q13.33DISEASEInfantile Striatonigral DegenerationREFERENCE10944103, 19689417ORGANNervous System,Eye,