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Publications by Ángeles Yahel Hernández-Vázquez

Leber Congenital Amaurosis RPE65: 7 Years Follow Up

Gaceta Medica de Mexico

English

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Results at 2 Years After Gene Therapy for RPE65-Deficient Leber Congenital Amaurosis and Severe Early-Childhood–Onset Retinal Dystrophy

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The Phenotype of Leber Congenital Amaurosis in Patients With AIPL1 Mutations

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Molecular and Clinical Analysis of 27 German Patients With Leber Congenital Amaurosis

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Hypomorphic Mutations Identified in the Candidate Leber Congenital Amaurosis Gene CLUAP1

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Nonpenetrance of the Most Frequent Autosomal Recessive Leber Congenital Amaurosis Mutation inNMNAT1

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Compound Heterozygous Novel Frameshift Variants in the PROM1 Gene Result in Leber Congenital Amaurosis

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Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients With Leber Congenital Amaurosis

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Mutation Screen of the TUB Gene in Patients With Retinitis Pigmentosa and Leber Congenital Amaurosis

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