Ya You
Zhengzhou, China
Last Updated: 09/26/2026
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Found 8 publications
Pathogenicity and Functional Analysis of Multi-Variant Allele of RPE65 Causing Retinitis Pigmentosa.
Pathogenicity and Functional Analysis of Multi-Variant Allele of RPE65 Causing Retinitis Pigmentosa.
Journal: Translational vision science & technology
Published: February 02, 2026
Pathogenicity and Function Analysis of Two Novel SLC4A11 Variants in Patients With Congenital Hereditary Endothelial Dystrophy.
Journal: Translational vision science & technology
Published: October 03, 2023
A novel mutation located in the intermembrane space domain of AFG3L2 causes dominant optic atrophy through decreasing the stability of the encoded protein.
Journal: Cell death discovery
Published: April 01, 2022
Phenotype Heterogeneity and the Association Between Visual Acuity and Outer Retinal Structure in a Cohort of Chinese X-Linked Juvenile Retinoschisis Patients.
Journal: Frontiers in genetics
Published: December 10, 2021
Autosomal Recessive Rod-Cone Dystrophy Associated With Compound Heterozygous Variants in ARL3 Gene.
Journal: Frontiers in cell and developmental biology
Published: November 30, 2020
Identification of Four Novel Variants and Determination of Genotype-Phenotype Correlations for ABCA4 Variants Associated With Inherited Retinal Degenerations.
Journal: Frontiers in cell and developmental biology
Published: November 29, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026