A Case of AOA2 With Compound Heterozygous SETX Mutations
J Mov Disord
.
2022 May;15(2):178-180.
doi: 10.14802/jmd.21139.
Epub 2021 Dec 24.
Authors
Hee Jin Chang
1
,
Ryul Kim
2
,
Minchae Kim
1
,
Jangsup Moon
1
3
,
Man Jin Kim
3
4
,
Han-Joon Kim
1
Affiliations
1
Department of Neurology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
2
Department of Neurology, Inha University Hospital, Incheon, Korea.
3
Rare Disease Center, Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.
4
Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
PMID:
34937158
PMCID:
PMC9171306
DOI:
10.14802/jmd.21139
No abstract available
Grants and funding
2020-ER6904-01/Korea Disease Control and Prevention Agency