Infantile parkinsonism‐dystonia: Tyrosine hydroxylase deficiency

Publisher Website

1 March 1998

journal article
editorial
Published by Wiley in Movement Disorders

Vol. 13 (2) , 350
https://doi.org/10.1002/mds.870130226

Abstract

No abstract available

This publication has 1 reference indexed in Scilit:

Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene
Human Molecular Genetics, 1996