Tyrosine hydroxylase deficiency unresponsive to L-DOPA treatment with unusual clinical and biochemical presentation.

Authors :: Lonlay, P. de
Nassogne, M.C.
Gennip, A.H. van
Cruchten, A.C. van
Bilette de Villemeur, T.
Cretz, M.
Stoll, C.
Launay, J.M.
Steenbergen-Spanjers, G.C.H.
Heuvel, L.P.W.J. van den
Wevers, R.A.
Saudubray, J.M.
Abeling, N.G.G.M.
Lonlay, P. de
Nassogne, M.C.
Gennip, A.H. van
Cruchten, A.C. van
Bilette de Villemeur, T.
Cretz, M.
Stoll, C.
Launay, J.M.
Steenbergen-Spanjers, G.C.H.
Heuvel, L.P.W.J. van den
Wevers, R.A.
Saudubray, J.M.
Abeling, N.G.G.M.
Source :: Journal of Inherited Metabolic Disease; 819; 825; 0141-8955; 23; ~Journal of Inherited Metabolic Disease~819~825~~~0141-8955~~23~~
Publication Year :: 2000
Abstract: Item does not contain fulltext

Database :: OAIster
Journal :: Journal of Inherited Metabolic Disease; 819; 825; 0141-8955; 23; ~Journal of Inherited Metabolic Disease~819~825~~~0141-8955~~23~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1367144171
Document Type :: Electronic Resource

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