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Mutation spectrum of <i>NDP</i>, <i>FZD4</i> and <i>TSPAN12</i> genes in Indian patients with retinopathy of prematurity

14

Citations

21

References

2017

Year

Abstract

This is a first study that revealed association of few variants in Norrin signalling genes among Indian patients with ROP that warrants further detailed investigation worldwide.

References

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