白质营养不良
生物
氨基酰化
粒线体疾病
复合杂合度
白质
突变
病理
分子生物学
遗传学
转移RNA
线粒体DNA
医学
基因
核糖核酸
疾病
磁共振成像
放射科
作者
Marjo S. van der Knaap,Marianna Bugiani,Marisa I. Mendes,Lisa G. Riley,Desirée E.C. Smith,Joëlle Rudinger‐Thirion,Magali Frugier,Marjolein Breur,Joanna Crawford,Judith van Gaalen,Meyke Schouten,Marjolaine Willems,Quinten Waisfisz,Frédéric Tran Mau‐Them,Richard J. Rodenburg,Ryan J. Taft,Boris Keren,John Christodoulou,Christel Depienne,Cas Simons
出处
期刊:Neurology
[Lippincott Williams & Wilkins]
日期:2019-02-09
卷期号:92 (11): e1225-e1237
被引量:47
标识
DOI:10.1212/wnl.0000000000007098
摘要
This study adds LARS2 and KARS pathogenic variants as gene defects that may underlie deafness, ovarian failure, and leukodystrophy with mitochondrial signature. We discuss the specific MRI characteristics shared by leukodystrophies caused by mitochondrial tRNA synthase defects. We propose to add aminoacylation assays as biochemical diagnostic tools for leukodystrophies.
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