A Case of McLeod Syndrome with A Novel
XK
Missense Mutation
Mov Disord Clin Pract
.
2018 Apr 6;5(3):333-336.
doi: 10.1002/mdc3.12614.
eCollection 2018 May-Jun.
Authors
Hiroyasu Komiya
1
,
Mutsuki Takasu
1
2
,
Shunta Hashiguchi
1
,
Eri Uematsu
1
,
Ryoko Fukai
1
,
Kenichi Tanaka
1
,
Mikiko Tada
1
,
Hideto Joki
1
,
Tatsuya Takahashi
2
,
Shigeru Koyano
1
,
Hiroshi Doi
1
,
Hideyuki Takeuchi
1
,
Fumiaki Tanaka
1
Affiliations
1
Department of Neurology and Stroke Medicine Yokohama City University Graduate School of Medicine 3-9 Fukuura, Kanazawa-ku Yokohama, 236-0004 Japan.
2
Department of Neurology National Hospital Organization Yokohama Medical Center, Harajuku Totsuka-ku Yokohama, 245-8575 Japan.
PMID:
30800707
PMCID:
PMC6336288
DOI:
10.1002/mdc3.12614
No abstract available
Keywords:
McLeod syndrome; XK; chorea; missense mutation; neuroacanthocytosis; p.Arg222Pro.
Publication types
Case Reports