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Article

A Family of Fuchs Endothelial Corneal Dystrophy and Anterior Polar Cataract with An Analysis of Whole Exome Sequencing

2020-02-14

Abstract excerpt

<title>Abstract</title> <p><bold>Background</bold> Our aim was to introduce a family affected by this rare phenotype, and perform the whole exome sequencing (WES) to explore the potential candidate genes causing the disorders.<bold>Methods </bold>A five-generation family including 5 patients affected by FECD with APC, and 9 patients suffered from only FECD was recruited from the First Affiliated Hospital of Harbi...

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Literature Corpus work
9acc41b7-db20-51a0-a54c-ecd2fb64b7ff
DOI
10.21203/rs.2.23532/v1
Open publication

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