Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency? Response from the authors

Anthony E. Lang*, Julien F. Bally, David P. Breen, Susen Schaake, Joanne Trinh, Aleksandar Rakovic, Christine Klein

*Corresponding author for this work
Original languageEnglish
JournalParkinsonism and Related Disorders
Pages (from-to)80
Number of pages1
Publication statusPublished - 05.2020

Research Areas and Centers

  • Research Area: Medical Genetics

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