Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes

Authors :: Lenders, J.W.M.
Eisenhofer, G.
Abeling, N.G.G.M.
Berger, W.
Murphy, D.L.
Konings, H.
Bleeker-Wagemakers, P.L.M.
Kopin, I.J.
Karoum, F.
Gennip, A.H. van
Brunner, H.G.
Lenders, J.W.M.
Eisenhofer, G.
Abeling, N.G.G.M.
Berger, W.
Murphy, D.L.
Konings, H.
Bleeker-Wagemakers, P.L.M.
Kopin, I.J.
Karoum, F.
Gennip, A.H. van
Brunner, H.G.
Source :: Journal of Clinical Investigation; 1010; 1019; 0021-9738; 97; ~Journal of Clinical Investigation~1010~1019~~~0021-9738~~97~~
Publication Year :: 1996
Abstract: Item does not contain fulltext

Database :: OAIster
Journal :: Journal of Clinical Investigation; 1010; 1019; 0021-9738; 97; ~Journal of Clinical Investigation~1010~1019~~~0021-9738~~97~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1367213021
Document Type :: Electronic Resource

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