Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G>A and m.14484T>C of the mitochondrial DNA.
| Image |  |
|---|---|
| Description | scientific article published on 6 October 2016 |
| Author/s |
author: Claudia B. Catarino Holger Prokisch |
| Publication date | October 6, 2016 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |