Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia

Author:

Hoffmann Georg F.,Assmann Birgit,Br�utigam Christa,Dionisi-Vici Carlo,H�ussler Martin,De Klerk Johannes B. C.,Naumann Markus,Steenbergen-Spanjers Gerry C. H.,Strassburg Hans-Michael,Wevers Ron A.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference26 articles.

1. The biochemical basis of neuropharmacology. New York, Oxford: Oxford University Press, 1996: 230.

2. Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development

3. The hyperphenylalaninemias. Marburg, Germany: Tectum Verlag, 1996.

4. et al. An infant with clinical features, a metabolic profile and response to treatment suggestive of tyrosine hydroxylase deficiency. Poster presentation 49 at: 32nd Annual Symposium SSIEM; 1994; Edinburgh, UK.

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