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Mitochondrial DNA analysis in primary congenital glaucoma

PURPOSE: To screen mitochondrial DNA (mtDNA) for nucleotide variations in primary congenital glaucoma (PCG). METHODS: The entire coding region of the mitochondrial genome was amplified by polymerase chain reaction from 35 PCG patients and 40 controls. The full mtDNA genome except the D-loop was sequ...

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Autori principali: Tanwar, Mukesh, Dada, Tanuj, Sihota, Ramanjit, Dada, Rima
Natura: Artigo
Lingua:Inglês
Pubblicazione: Molecular Vision 2010
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2846849/
https://ncbi.nlm.nih.gov/pubmed/20361014
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