对芬斯特勒和扎鲁克 - 马赫朱卜发表于《临床肾脏病病例研究》2018年第6卷第1期的致编辑信的回复
Response to the Letter to the Editor by Finsterer and Zarrouk-Mahjoub in Clin Nephrol Case Stud. 2018; 6: 1.
作者信息
Lim Kenneth, Steele David, Fenves Andrew, Thadhani Ravi, Heher Eliot, Karaa Amel
机构信息
Division of Nephrology and.
Department of Genetics and Pediatrics, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
出版信息
Clin Nephrol Case Stud. 2018 Jan 16;6:2-3. doi: 10.5414/CNCS109366R. eCollection 2018.
Abstract
Not available.
摘要
无法提供。
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本文引用的文献
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Focal segmental glomerulosclerosis associated with mitochondrial disease.与线粒体疾病相关的局灶节段性肾小球硬化
Clin Nephrol Case Stud. 2017 Mar 3;5:20-25. doi: 10.5414/CNCS109083. eCollection 2017.
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Renal manifestations of primary mitochondrial disorders.原发性线粒体疾病的肾脏表现。
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PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspring.PGD 与异质线粒体 DNA 点突变：系统评价估计健康后代的机会。
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A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features.一个新的线粒体 tRNA(Trp)基因突变导致晚发性脑肌病，还有其他一些特征。
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Mitochondrial DNA mutations and human disease.线粒体DNA突变与人类疾病
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The not so 'mighty chondrion': emergence of renal diseases due to mitochondrial dysfunction.并非那么“强大”的线粒体：线粒体功能障碍导致的肾脏疾病的出现
Nephron Physiol. 2007;105(1):p1-10. doi: 10.1159/000096860. Epub 2006 Nov 8.
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Tissue specific distribution of the 3243A->G mtDNA mutation.3243A→G线粒体DNA突变的组织特异性分布。
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