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Publications by Janneke H. M. Schuurs-Hoeijmakers

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

JAMA Ophthalmology

English

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Leber Congenital Amaurosis RPE65: 7 Years Follow Up

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The Phenotype of Leber Congenital Amaurosis in Patients With AIPL1 Mutations

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Hypomorphic Mutations Identified in the Candidate Leber Congenital Amaurosis Gene CLUAP1

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

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A Novel Missence Mutation in the Transglutaminase-1 Gene in an Autosomal Recessive Congenital Ichthyosis Patient

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