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Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation

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Year: 2008
Type: article
Study design: Observational Study
Source: Journal of genetics and genomics/Journal of Genetics and Genomics
DOI: 10.1016/s1673-8527(08)60086-7
Authors: Wanshi Cai, Qun Fu, Xiangtian Zhou, Jia Qu, Yi Tong, Min-Xin Guan
Institutions: Wenzhou Medical University, Henan Medical University, Fujian Medical University, First Affiliated Hospital of Fujian Medical University, Cincinnati Children's Hospital Medical Center
Language: English

Topic: Mitochondrial Function and Pathology
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W2052339493
FWCI: 1.008
Cites: 27
Cited by: 57
Related to: 10
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