Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber’s hereditary optic neuropathy-associated mitochondrial DNA mutation-Reference-Cited by-同舟云学术

Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber’s hereditary optic neuropathy-associated mitochondrial DNA mutation

Published:2016-07-17 Issue:16 Volume:25 Page:3613-3625
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Jiang Pingping,Liang Min,Zhang Chaofan,Zhao Xiaoxu,He Qiufen,Cui Limei,Liu Xiaoling,Sun Yan-Hong,Fu Qun,Ji Yanchun,Bai Yidong,Huang Taosheng,Guan Min-Xin

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference68 articles.

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2. Clinical Picture of LHON;Nikoskelainen;Clin. Neurosci,1994

3. Inherited mitochondrial optic neuropathies

4. Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders

5. Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy;Wallace;Science,1998

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