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Dive into the research topics of 'Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?'. Together they form a unique fingerprint.- Sort by
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Julien F. Bally, David P. Breen, Susen Schaake, Joanne Trinh, Aleksandar Rakovic, Christine Klein, Anthony E. Lang*