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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Detaylı Bibliyografya
Asıl Yazarlar: Kumar, Manoj, Tanwar, Mukesh, Faiq, Muneeb Ahmad, Pani, Jhumur, Shamsi, Monis Bilal, Dada, Tanuj, Dada, Rima
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Molecular Vision 2013
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3566903/
https://ncbi.nlm.nih.gov/pubmed/23401651
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