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Familial Intracranial Aneurysm Requires Not Only Whole-Exome Sequencing, But Also Mitochondrial DNA Sequencing.

作者信息

Finsterer Josef

机构信息

Neurology & Neurophysiology Center, Vienna, Austria.

出版信息

Korean J Radiol. 2022 May;23(5):566-567. doi: 10.3348/kjr.2022.0029.

Abstract
摘要

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本文引用的文献

1
Whole Exome Sequencing in Patients with Phenotypically Associated Familial Intracranial Aneurysm.
Korean J Radiol. 2022 Jan;23(1):101-111. doi: 10.3348/kjr.2021.0467. Epub 2021 Oct 1.
2
Role of myeloperoxidase in abdominal aortic aneurysm formation: mitigation by taurine.
Am J Physiol Heart Circ Physiol. 2017 Dec 1;313(6):H1168-H1179. doi: 10.1152/ajpheart.00296.2017. Epub 2017 Sep 29.
3
Late onset MELAS with m.3243A > G mutation and its association with aneurysm formation.
Metab Brain Dis. 2017 Aug;32(4):1069-1072. doi: 10.1007/s11011-017-9989-0. Epub 2017 Mar 21.
4
Association between polymorphisms in the interleukin-10 gene and risk of abdominal aortic aneurysm.
Genet Mol Res. 2015 Dec 21;14(4):17599-604. doi: 10.4238/2015.December.21.32.
5
6
Association between three eNOS polymorphisms and intracranial aneurysms risk: a meta-analysis.
Medicine (Baltimore). 2015 Jan;94(4):e452. doi: 10.1097/MD.0000000000000452.
7
Meta-analysis of the association between angiotensin-converting enzyme I/D polymorphism and aortic aneurysm risk.
J Renin Angiotensin Aldosterone Syst. 2015 Dec;16(4):1125-9. doi: 10.1177/1470320314545557. Epub 2014 Aug 25.
8
A polymorphic variant of the endoglin gene is associated with increased risk for intracranial aneurysms in a Korean population.
Surg Neurol. 2008 Jul;70(1):39-44. doi: 10.1016/j.surneu.2008.01.060. Epub 2008 Apr 28.
9
Aortic rupture in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes.
Arch Neurol. 2006 Feb;63(2):281-3. doi: 10.1001/archneur.63.2.281.
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Mitochondrial-dependent apoptosis in experimental rodent abdominal aortic aneurysms.
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