A Novel Autosomal Recessive Variant of the <i>NRL</i> Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients
Enhanced S-cone syndrome (ESCS) is a rare autosomal recessive retinal degeneration mainly associated with pathogenic variations in the <i>NR2E3</i> gene. Only a few pathogenic variations in the <i>NRL</i> gene associated with ESCS have been reported to date. Here, we describe...
Main Authors: | , , , , , , , , , , , |
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格式: | 文件 |
语言: | English |
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MDPI AG
2022-09-01
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丛编: | Diagnostics |
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在线阅读: | https://www.mdpi.com/2075-4418/12/9/2183 |