| Literature DB >> 27847334 |
Elona Jankauskaitė1, Ewa Bartnik2, Agata Kodroń3.
Abstract
Leber's hereditary optic neuropathy (LHON) was the first human disease found to be associated with a mitochondrial DNA (mtDNA) point mutation. The most common LHON mutations are 11778G>A, 3460G>A or 14484T>C. The most common clinical features of LHON are optic nerve and retina atrophy. The affected tissue is not available for studies, therefore a variety of other cell types are used. However, all models face difficulties and limitations in mitochondrial disease research. The advantages and disadvantages of different cell models used to study LHON, recent advances in animal model generation and novel approaches in this field are discussed.Entities:
Keywords: Cell line models; Leber's hereditary optic neuropathy; Mitochondrial DNA; Mitochondrial genome editing; Retinal ganglion cells
Mesh:
Year: 2016 PMID: 27847334 DOI: 10.1016/j.mito.2016.11.006
Source DB: PubMed Journal: Mitochondrion ISSN: 1567-7249 Impact factor: 4.160