Incidence of PAX6 single nucleotide polymorphisms in congenital iridofundal coloboma and other congenital ocular abnormalities: a tertiary care hospital experience from central India

Incidence of PAX6 single nucleotide polymorphisms in congenital iridofundal coloboma and other congenital ocular abnormalities: a tertiary care hospital experience from central India

Purpose of this study is to identify selected single nucleotide polymorphisms (SNP) of the PAX6 gene and to assess their correlation with congenital iridofundal colobomas and other congenital ocular anomalies.Material and methods. It was a case-control study done on 45 patients aged from 75 days to...

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Bibliographic Details
Main Authors: Sh. Jain, S. Lakhtakia, P. Choudhary, S. K. Pandey, Sh. L. Chandravanshi, A. Tiwari
Format: Article
Language:Russian
Published: Real Time Ltd 2024-12-01
Series:Российский офтальмологический журнал
Subjects:
polymorphism
mutation
gene
polymerase chain reaction
restriction fragment length polymorphism
single-nucleotide polymorphism
Online Access:https://roj.igb.ru/jour/article/view/1626

Internet

https://roj.igb.ru/jour/article/view/1626

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