Biochemical and molecular genetic characteristics of the severe form of tyrosine hydroxylase deficiency.

Authors :: Brautigam, C.
Steenbergen-Spanjers, G.C.H.
Hoffmann, G.F.
Dionisi-Vici, C.
Heuvel, L.P.W.J. van den
Smeitink, J.A.M.
Wevers, R.A.
Brautigam, C.
Steenbergen-Spanjers, G.C.H.
Hoffmann, G.F.
Dionisi-Vici, C.
Heuvel, L.P.W.J. van den
Smeitink, J.A.M.
Wevers, R.A.
Source :: Clinical Chemistry; 2073; 2078; 0009-9147; 12; 45; ~Clinical Chemistry~2073~2078~~~0009-9147~12~45~~
Publication Year :: 1999
Abstract: Item does not contain fulltext

Database :: OAIster
Journal :: Clinical Chemistry; 2073; 2078; 0009-9147; 12; 45; ~Clinical Chemistry~2073~2078~~~0009-9147~12~45~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1284048526
Document Type :: Electronic Resource

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