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Items: 8

1.

The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation.

Qian Y, Zhou X, Liang M, Qu J, Guan MX.

Mitochondrion. 2011 Nov;11(6):871-7. doi: 10.1016/j.mito.2011.06.006. Epub 2011 Jul 1.

PMID:
21742061
2.

[The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].

Mao YJ, Qu J, Guan MX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Feb;25(1):45-9. Review. Chinese.

PMID:
18247303
3.

Leber's hereditary optic neuropathy: a multifactorial disease.

Yen MY, Wang AG, Wei YH.

Prog Retin Eye Res. 2006 Jul;25(4):381-96. Epub 2006 Jul 7. Review.

PMID:
16829155
4.

Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration.

Carelli V, Rugolo M, Sgarbi G, Ghelli A, Zanna C, Baracca A, Lenaz G, Napoli E, Martinuzzi A, Solaini G.

Biochim Biophys Acta. 2004 Jul 23;1658(1-2):172-9. Review.

5.

mtDNA mutations in Leber's hereditary optic neuropathy.

Savontaus ML.

Biochim Biophys Acta. 1995 May 24;1271(1):261-3. Review.

PMID:
7599218
6.

Leber hereditary optic neuropathy.

Y-W-Man P, Turnbull DM, Chinnery PF.

J Med Genet. 2002 Mar;39(3):162-9. Review.

7.

Mitochondrial genetic control of assembly and function of complex I in mammalian cells.

Chomyn A.

J Bioenerg Biomembr. 2001 Jun;33(3):251-7. Review.

PMID:
11695835
8.

Identification of the variants in PARL, the nuclear modifier gene, responsible for the expression of LHON patients in Thailand.

Istikharah R, Tun AW, Kaewsutthi S, Aryal P, Kunhapan B, Katanyoo W, Chuenkongkaew W, Lertrit P.

Exp Eye Res. 2013 Nov;116:55-7. doi: 10.1016/j.exer.2013.08.007. Epub 2013 Aug 22. Review.

PMID:
23973714
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