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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Detalles Bibliográficos
Autores principales: Tanwar, Mukesh, Dada, Tanuj, Sihota, Ramanjit, Dada, Rima
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846849/
https://www.ncbi.nlm.nih.gov/pubmed/20361014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846849/
https://www.ncbi.nlm.nih.gov/pubmed/20361014

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