A carregar...
Leber hereditary optic neuropathy: bridging the translational gap
PURPOSE OF REVIEW: Leber hereditary optic neuropathy (LHON) is the most common primary mitochondrial DNA (mtDNA) genetic disorder in the population. We address the clinical evolution of the disease, the secondary etiological factors that could contribute to visual loss, and the challenging task of d...
Na minha lista:
| Publicado no: | Curr Opin Ophthalmol |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Lippincott Williams & Wilkins
2017
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5562441/ https://ncbi.nlm.nih.gov/pubmed/28650878 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/ICU.0000000000000410 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|