Suppr超能文献

mtDNA mutations that cause optic neuropathy: how do we know?

作者信息

Howell N, Bogolin C, Jamieson R, Marenda D R, Mackey D A

出版信息

Am J Hum Genet. 1998 Jan;62(1):196-202. doi: 10.1086/301675.

Abstract
摘要

引用本文的文献

1
Establishing risk of vision loss in Leber hereditary optic neuropathy.
Am J Hum Genet. 2021 Nov 4;108(11):2159-2170. doi: 10.1016/j.ajhg.2021.09.015. Epub 2021 Oct 19.
2
Leber hereditary optic neuropathy-new insights and old challenges.
Graefes Arch Clin Exp Ophthalmol. 2021 Sep;259(9):2461-2472. doi: 10.1007/s00417-020-04993-1. Epub 2020 Nov 13.
7
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy.
PLoS One. 2012;7(8):e42242. doi: 10.1371/journal.pone.0042242. Epub 2012 Aug 3.
8
Leber's Hereditary Optic Neuropathy-Gene Therapy: From Benchtop to Bedside.
J Ophthalmol. 2011;2011:179412. doi: 10.1155/2011/179412. Epub 2010 Dec 26.
9
Inherited mitochondrial optic neuropathies.
J Med Genet. 2009 Mar;46(3):145-58. doi: 10.1136/jmg.2007.054270. Epub 2008 Nov 10.
10
The role of the Met98Lys optineurin variant in inherited optic nerve diseases.
Br J Ophthalmol. 2006 Nov;90(11):1420-4. doi: 10.1136/bjo.2006.099333. Epub 2006 Aug 2.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验