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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Science Planet Inc.
2017-10-01
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Series: | Canadian Journal of Biotechnology |
Online Access: | https://www.canadianjbiotech.com/CAN_J_BIOTECH/Archives/v1/Special Issue/cjb.2017-a78.pdf |