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A study on genetic copy number variations reveals NLGN1 is over represented in primary angle closure glaucoma patients

2024-12-10

Abstract excerpt

<title>Abstract</title> <p><bold>Introduction: </bold>Primary angle closure glaucoma (PACG) is one of the leading causes of blindness worldwide with a complex genetic etiology. For complex genetic disorders, copy number variation (CNV) is anticipated to play an essential role in disease vulnerability. The impact of CNVs on PACG has not been studied yet. <bold>Methods:</bold> In India, ~30% of people show narrow a...

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Literature Corpus work: c4b2adea-22d1-502e-afeb-7250b4e84bc0
DOI: 10.21203/rs.3.rs-5406735/v1

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