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A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population
L. P. W. J. van den Heuvel, Bernadette Luiten, J. A. M. Smeitink, Johanneke F. de Rijk-van Andel, Keith Hyland, Gerry C. H. Steenbergen-Spanjers, R. J. T. Janssen, R. A. WeversVolume:
102
Language:
english
Pages:
3
DOI:
10.1007/s004390050756
Date:
July, 1998
File:
PDF, 73 KB
english, 1998