An adult patient with 3-methylglutaconic aciduria type 1 and movement disorders
J Neurol
.
2022 Jul;269(7):3915-3917.
doi: 10.1007/s00415-022-10999-y.
Epub 2022 Feb 3.
Authors
M Mainardi
1
,
L Lerjefors
1
,
G Bonato
1
,
C Bertolin
2
,
L Salviati
2
,
M Carecchio
3
Affiliations
1
Movement Disorders Unit, Department of Neuroscience, University of Padua, Via Giustiniani 2, 35128, Padua, Italy.
2
Clinical Genetics Unit, Department of Woman and Child Health, University of Padua, Via Giustiniani 3, 35127, Padua, Italy.
3
Movement Disorders Unit, Department of Neuroscience, University of Padua, Via Giustiniani 2, 35128, Padua, Italy. miryam.carecchio@unipd.it.
PMID:
35113260
DOI:
10.1007/s00415-022-10999-y
No abstract available
Publication types
Letter
MeSH terms
Adult
Humans
Metabolism, Inborn Errors*
Movement Disorders* / etiology
Supplementary concepts
3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria, Type I