APA

van den Heuvel L. P., Luiten B., Smeitink J. A., de Rijk-van Andel J. F., Hyland K., Steenbergen-Spanjers G. C., Janssen R. J. & Wevers R. A. (19980818). A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population. : Human genetics.

Chicago

van den Heuvel L P, Luiten B, Smeitink J A, de Rijk-van Andel J F, Hyland K, Steenbergen-Spanjers G C, Janssen R J and Wevers R A. 19980818. A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population. : Human genetics.

Harvard

van den Heuvel L. P., Luiten B., Smeitink J. A., de Rijk-van Andel J. F., Hyland K., Steenbergen-Spanjers G. C., Janssen R. J. and Wevers R. A. (19980818). A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population. : Human genetics.

MLA

van den Heuvel L P, Luiten B, Smeitink J A, de Rijk-van Andel J F, Hyland K, Steenbergen-Spanjers G C, Janssen R J and Wevers R A. A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population. : Human genetics. 19980818.