Varying neurological phenotypes amongmut° andmut− patients with methylmalonylCoA mutase deficiency
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference32 articles.
1. (1982) “Neurology of Hereditary Metabolic Diseases of Children.” New York: McGraw-Hill.
2. Experimental vitamin B12 deficiency: Its effect on tissue vitamin B12-coenzyme levels and on the metabolism of methylmalonyl-CoA
3. METHYLMALONIC ACID EXCRETION: AN INDEX OF VITAMIN-B12 DEFICIENCY
4. Cloning and expression of a mutant methylmalonyl coenzyme A mutase with altered cobalamin affinity that causes mut- methylmalonic aciduria.
5. Phenotype of disease in three patients with identical mutations in methylmalonyl CoA mutase
Cited by 55 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The Regulation and Characterization of Mitochondrial-Derived Methylmalonic Acid in Mitochondrial Dysfunction and Oxidative Stress: From Basic Research to Clinical Practice;Oxidative Medicine and Cellular Longevity;2022-05-24
2. Review of neuropsychological outcomes in isolated methylmalonic acidemia: recommendations for assessing impact of treatments;Metabolic Brain Disease;2022-03-29
3. MUT gene variants in patients with methylmalonic acidemia in Bangladeshi population and their distinguishing metabolic profiles;Meta Gene;2021-12
4. Inactivity of Peptidase ClpP Causes Primary Accumulation of Mitochondrial Disaggregase ClpX with Its Interacting Nucleoid Proteins, and of mtDNA;Cells;2021-11-29
5. Fooled by the fragments: vitamin B12 deficiency masquerading as thrombotic thrombocytopenic purpura;Journal of Community Hospital Internal Medicine Perspectives;2021-05-04
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3