(Q47690346)
Statements
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A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population (English)
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van den Heuvel LP
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Luiten B
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Smeitink JA
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de Rijk-van Andel JF
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Hyland K
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Steenbergen-Spanjers GC
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Janssen RJ
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1 June 1998
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102
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6
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644-646
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