Basal Ganglia Syndrome in a Male With an XK Gene Variant but Without XK Disease (McLeod Syndrome)
J Mov Disord
.
2024 Apr;17(2):226-229.
doi: 10.14802/jmd.23196.
Epub 2024 Jan 8.
Authors
Jeryl Ritzi T Yu
1
2
,
Ruth H Walker
3
,
Adrian Danek
4
,
Connie M Westhoff
5
,
Sunitha Vege
5
,
Ilia Itin
6
Affiliations
1
Institute for Neurosciences, St. Luke's Medical Center, Quezon City and Global City, Philippines.
2
University of the East, Ramon Magsaysay Memorial Medical Center, Quezon City, Philippines.
3
James J. Peters VA Medical Center, Bronx; Mount Sinai School of Medicine, New York, NY, USA.
4
Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.
5
New York Blood Center, New York, NY, USA.
6
Center for Neurological Restoration, Cleveland Clinic, Cleveland, OH, USA.
PMID:
38185097
PMCID:
PMC11082608
DOI:
10.14802/jmd.23196
No abstract available
Grants and funding
01GM1003/European Multidisciplinary Initiative on Neuroacanthocytosis
Ludwig-Maximilians-Universität Munich, Germany