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Publications by Helen Mintz-Hittner

Prevalence of Mutations Causing Retinitis Pigmentosa and Other Inherited Retinopathies

English

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Perspective on Genes and Mutations Causing Retinitis Pigmentosa

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NMNAT1 Mutation Causing Retinitis Pigmentosa

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Novel Mutations in PRPF31 Causing Retinitis Pigmentosa Identified Using Whole-Exome Sequencing

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High Prevalence of Mutations in theEYSGene in Japanese Patients With Autosomal Recessive Retinitis Pigmentosa

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Rhodopsin Mutations in Chinese Patients With Retinitis Pigmentosa

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Mutations in USH2A in Spanish Patients With Autosomal Recessive Retinitis Pigmentosa: High Prevalence and Phenotypic Variation

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High Prevalence of Mutations Affecting the Splicing Process in a Spanish Cohort With Autosomal Dominant Retinitis Pigmentosa

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Unilateral Retinitis Pigmentosa: Case Report

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British Retinitis Pigmentosa Society (BRPS)

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