Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency? Response from the authors
Details
Serval ID
serval:BIB_466CC72206C4
Type
Article: article from journal or magazin.
Publication sub-type
Letter (letter): Communication to the publisher.
Collection
Publications
Institution
Title
Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency? Response from the authors
Journal
Parkinsonism Relat Disord
ISSN
1873-5126 (Electronic)
ISSN-L
1353-8020
Publication state
Published
Issued date
05/2020
Volume
74
Pages
80
Language
english
Notes
Lang, Anthony E
Bally, Julien F
Breen, David P
Schaake, Susen
Trinh, Joanne
Rakovic, Aleksandar
Klein, Christine
eng
Letter
Comment
England
Parkinsonism Relat Disord. 2020 May;74:80. doi: 10.1016/j.parkreldis.2020.03.026. Epub 2020 Apr 9.
Bally, Julien F
Breen, David P
Schaake, Susen
Trinh, Joanne
Rakovic, Aleksandar
Klein, Christine
eng
Letter
Comment
England
Parkinsonism Relat Disord. 2020 May;74:80. doi: 10.1016/j.parkreldis.2020.03.026. Epub 2020 Apr 9.
Keywords
*Dystonic Disorders, Heterozygote, Humans, Mutation, Tyrosine 3-Monooxygenase/*genetics, *Autosomal recessive, *Dopa-responsive, *Dystonia, *Heterozygote, *Tyrosine hydroxylase
Pubmed
Create date
21/05/2021 9:09
Last modification date
22/05/2021 5:34
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