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

doi:10.1016/j.parkreldis.2020.03.026

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

Institute of Neurogenetics

2 Citations (Scopus)

Original language	English
Journal	Parkinsonism and Related Disorders
Volume	74
Pages (from-to)	80
Number of pages	1
ISSN	1353-8020
DOIs	https://doi.org/10.1016/j.parkreldis.2020.03.026
Publication status	Published - 05.2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

Research Areas and Centers

Research Area: Medical Genetics

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10.1016/j.parkreldis.2020.03.026

Cite this

@article{299b134536b347ee9ce8ce2f42b2ab8f,

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

author = "Lang, \{Anthony E.\} and Bally, \{Julien F.\} and Breen, \{David P.\} and Susen Schaake and Joanne Trinh and Aleksandar Rakovic and Christine Klein",

year = "2020",

month = may,

doi = "10.1016/j.parkreldis.2020.03.026",

language = "English",

volume = "74",

pages = "80",

journal = "Parkinsonism and Related Disorders",

issn = "1353-8020",

publisher = "Elsevier Ltd",

}

TY - JOUR

T1 - Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency? Response from the authors

AU - Lang, Anthony E.

AU - Bally, Julien F.

AU - Breen, David P.

AU - Schaake, Susen

AU - Trinh, Joanne

AU - Rakovic, Aleksandar

AU - Klein, Christine

PY - 2020/5

Y1 - 2020/5

UR - https://www.scopus.com/pages/publications/85086341154

U2 - 10.1016/j.parkreldis.2020.03.026

DO - 10.1016/j.parkreldis.2020.03.026

M3 - Letters

C2 - 32305180

AN - SCOPUS:85086341154

SN - 1353-8020

VL - 74

SP - 80

JO - Parkinsonism and Related Disorders

JF - Parkinsonism and Related Disorders

ER -

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

UN SDGs

Research Areas and Centers

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