A Novel c19orf12 Mutation in Mitochondrial Membrane Protein-Associated Neurodegeneration

被引：1
作者：
Nobile, Steven [1 ]
Thulasirajah, Salini [2 ]
Venkateswaran, Sunita [2 ]
机构：
[1] Univ Laval, Hop Enfant Jesus, Ctr Hosp Univ Quebec, Dept Neurol, Quebec City, PQ, Canada
[2] Univ Ottawa, Childrens Hosp Eastern Ontario, Dept Neurol, Ottawa, ON, Canada
来源：
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES | 2019年 / 46卷 / 05期
关键词：
Neurodegenerative disorders; Spasticity; Dementia; Magnetic resonance imaging; Molecular genetics; Pediatric neurology; MPAN; NBIA; C19ORF12; SPASTIC PARAPLEGIAS; IRON; PHENOTYPES; DISORDERS; FEATURES; GENETICS; SUBTYPE;
D O I：
10.1017/cjn.2019.224
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
[No abstract available]
引用
收藏
页码：610 / 614
页数：5
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