A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC). | J Inherit Metab Dis;22(4): 364-73, 1999 Jun. | MEDLINE

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A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC).

Wevers, R A; de Rijk-van Andel, J F; Bräutigam, C; Geurtz, B; van den Heuvel, L P; Steenbergen-Spanjers, G C; Smeitink, J A; Hoffmann, G F; Gabreëls, F J.

Affiliation

Wevers RA; Institute of Neurology, University Hospital Nijmegen, The Netherlands. R.Wevers@ckslkn.azn.nl

J Inherit Metab Dis ; 22(4): 364-73, 1999 Jun.

Article in En | MEDLINE | ID: mdl-10407773

Subject(s)

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Collection: 01-internacional Database: MEDLINE Main subject: Tyrosine 3-Monooxygenase / Mutation Type of study: Guideline Limits: Humans Language: En Journal: J Inherit Metab Dis Year: 1999 Document type: Article Affiliation country: Country of publication:

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Collection: 01-internacional Database: MEDLINE Main subject: Tyrosine 3-Monooxygenase / Mutation Type of study: Guideline Limits: Humans Language: En Journal: J Inherit Metab Dis Year: 1999 Document type: Article Affiliation country: Country of publication: