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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Detalles Bibliográficos
Autores principales: Kumar, Manoj, Tanwar, Mukesh, Faiq, Muneeb Ahmad, Pani, Jhumur, Shamsi, Monis Bilal, Dada, Tanuj, Dada, Rima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566903/
https://www.ncbi.nlm.nih.gov/pubmed/23401651

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566903/
https://www.ncbi.nlm.nih.gov/pubmed/23401651

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