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Publications by Britta Feldhaus

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

PLoS ONE
Multidisciplinary
2018English

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The Phenotype of Leber Congenital Amaurosis in Patients With AIPL1 Mutations

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Correction: Leber Congenital Amaurosis/Early-Onset Severe Retinal Dystrophy: Clinical Features, Molecular Genetics and Therapeutic Interventions

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

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Leber Congenital Amaurosis RPE65: 7 Years Follow Up

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

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Hypomorphic Mutations Identified in the Candidate Leber Congenital Amaurosis Gene CLUAP1

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Clinical and Genetic Characteristics of Leber Congenital Amaurosis in the Tunisian Population: Experience of the Oculogenetic Laboratory LR14SP01

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

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