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Caring for Hereditary Childhood Retinal Blindness.Clustered Regularly Interspaced Short Palindromic Repeats-Based Genome Surgery for the Treatment of Autosomal Dominant Retinitis Pigmentosa.Gene therapy in inherited retinal degenerative diseases, a reviewQuantitative progression of retinitis pigmentosa by optical coherence tomography angiographyMissense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesityHyperautofluorescent Dots are Characteristic in Ceramide Kinase Like-associated Retinal DegenerationMultimodal characterization of a novel mutation causing vitamin B6-responsive gyrate atrophyDeferoxamine-induced electronegative ERG responsesTwo-year progression analysis of RPE65 autosomal dominant retinitis pigmentosaPhenotypic expansion of autosomal dominant retinitis pigmentosa associated with the D477G mutation in RPE65Genetic Rescue Reverses Microglial Activation in Preclinical Models of Retinitis PigmentosaQuasidominance in autosomal recessive RDH12-Leber congenital amaurosisQuantitative Comparison of Near-infrared Versus Short-wave Autofluorescence Imaging in Monitoring Progression of Retinitis PigmentosaSCAPER-associated nonsyndromic autosomal recessive retinitis pigmentosaRates of Bone Spicule Pigment Appearance in Patients With Retinitis Pigmentosa Sine PigmentoStructural disease progression in PDE6-associated autosomal recessive retinitis pigmentosaOptical Coherence Tomography Angiography of RPGR-Associated Retinitis Pigmentosa Suggests Foveal Avascular Zone is a Biomarker for Vision LossCorrelation between B-scan optical coherence tomography, en face thickness map ring and hyperautofluorescent ring in retinitis pigmentosa patientsSpectrum of Disease Severity and Phenotype in Choroideremia Carriers
P50
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P50
description
researcher
@en
wetenschapper
@nl
name
Ruben Jauregui
@en
Ruben Jauregui
@nl
type
label
Ruben Jauregui
@en
Ruben Jauregui
@nl
prefLabel
Ruben Jauregui
@en
Ruben Jauregui
@nl
P31
P496
0000-0002-2367-7298