A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population

Author： van den Heuvel L. P. W. J.   Luiten Bernadette   Smeitink J. A. M.   de Rijk-van Andel Johanneke F.   Hyland Keith   Steenbergen-Spanjers Gerry C. H.   Janssen R. J. T.   Wevers R. A.  

Publisher： Springer Publishing Company

ISSN： 0340-6717

Source： Human Genetics, Vol.102, Iss.6, 1998-07, pp. : 644-646

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