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Mitochondrial DNA nucleotide changes in primary congenital glaucoma patients
PURPOSE: Primary congenital glaucoma (PCG) is the second most common cause of blindness, accounting for 0.01%–0.04% of total blindness worldwide. Most congenital glaucoma cases are mapped to the GLC3A locus, and many aspects of PCG are still unknown. Recent studies have reported an increased frequen...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Molecular Vision
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3566903/ https://ncbi.nlm.nih.gov/pubmed/23401651 |
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