Targeted next generation sequencing identifies novel mutations in Indian patients with retinal dystrophies

Retinal dystrophies (RD) are a group of inherited ocular disorders of the retina causing blindness in more than 2 million people worldwide. RDs are characterized by clinical variability and progressive vision loss. It is associated with high degree of genetic heterogeneity. In order to correlate RDs...

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Bibliographic Details
Main Authors: Rajeshwari Patil, Poornachandra Poornachandra, Nallathambi Jeyabalan, Arkasubhra Ghosh, Anuprita Ghosh
Format: Article
Language:English
Published: Science Planet Inc. 2017-10-01
Series:Canadian Journal of Biotechnology
Online Access:https://www.canadianjbiotech.com/CAN_J_BIOTECH/Archives/v1/Special Issue/cjb.2017-a78.pdf