New recessive compound heterozygous variants of RP1L1 in RP1L1 maculopathy

AIM: To identify a maculopathy patient caused by new recessive compound heterozygous variants in RP1L1. METHODS: Comprehensive retinal morphological and functional examinations were evaluated for the patient with RP1L1 maculopathy. Targeted sequence capture array technique was used to screen potenti...

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Bibliographic Details
Main Authors: Wen-Chao Cao, Qing-Shan Chen, Run Gan, Tao Huang, Xiao-He Yan
Format: Article
Language:English
Published: Press of International Journal of Ophthalmology (IJO PRESS) 2024-01-01
Series:International Journal of Ophthalmology
Subjects:
Online Access:http://ies.ijo.cn/en_publish/2024/1/20240114.pdf