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Comments on: Outer retinal tubulation and inner retinal pseudocysts in a patient with maternally inherited diabetes and deafness evaluated with optical coherence tomography angiogram.

作者信息

Finsterer Josef

机构信息

Krankenanstalt Rudolfstiftung, Messerli Institute, Vienna, Wien, Austria.

出版信息

Indian J Ophthalmol. 2020 Jul;68(7):1509-1510. doi: 10.4103/ijo.IJO_2358_19.

DOI:10.4103/ijo.IJO_2358_19
PMID:32587230
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7574117/
Abstract
摘要

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Comments on: Outer retinal tubulation and inner retinal pseudocysts in a patient with maternally inherited diabetes and deafness evaluated with optical coherence tomography angiogram.对以下内容的评论:一名患有母系遗传性糖尿病和耳聋的患者经光学相干断层扫描血管造影评估后的视网膜外层管状结构和视网膜内层假性囊肿
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引用本文的文献

1
Response to comments on: Outer retinal tubulation and inner retinal pseudocysts in a patient with maternally inherited diabetes and deafness evaluated with optical coherence tomography angiogram.对关于“通过光学相干断层扫描血管造影评估的母系遗传糖尿病和耳聋患者的外层视网膜管状结构和内层视网膜假性囊肿”评论的回复
Indian J Ophthalmol. 2020 Jul;68(7):1510-1511. doi: 10.4103/ijo.IJO_416_20.

本文引用的文献

1
Outer retinal tubulation and inner retinal pseudocysts in a patient with maternally inherited diabetes and deafness evaluated with optical coherence tomography angiogram.光学相干断层扫描血管造影评估母系遗传性糖尿病和耳聋患者的外视网膜小管化和内视网膜假囊肿。
Indian J Ophthalmol. 2020 Jan;68(1):250-253. doi: 10.4103/ijo.IJO_577_19.
2
Maternally inherited coronary heart disease is associated with a novel mitochondrial tRNA mutation.母系遗传的冠心病与一种新的线粒体tRNA突变有关。
BMC Cardiovasc Disord. 2019 Dec 16;19(1):293. doi: 10.1186/s12872-019-01284-4.
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Heteroplasmy and phenotype spectrum of the mitochondrial tRNA gene m.3243A>G mutation in seven Han Chinese families.七个汉族家系中线粒体 tRNA 基因 m.3243A>G 突变的异质性和表型谱。
J Neurol Sci. 2020 Jan 15;408:116562. doi: 10.1016/j.jns.2019.116562. Epub 2019 Nov 6.
4
Genetic Counselling for Maternally Inherited Mitochondrial Disorders.母系遗传线粒体疾病的遗传咨询
Mol Diagn Ther. 2017 Aug;21(4):419-429. doi: 10.1007/s40291-017-0279-7.
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A novel mitochondrial DNA m.7507A>G mutation is only pathogenic at high levels of heteroplasmy.
Neuromuscul Disord. 2015 Mar;25(3):262-7. doi: 10.1016/j.nmd.2014.11.002. Epub 2014 Nov 13.