Retinosis pigmentaria con herencia recesiva ligada al cromosoma x: caracterización oftalmológica
Ramírez Castro, Tomás; Lorenzo González, María E; Hernández Baguer, Raisa.
Rev. cuba. oftalmol
; 16(2)jul.-dic. 2003. tab, graf
Artículo en Español | LILACS | ID: lil-388420
Documentos relacionados
Retinitis Pigmentosa: From Pathomolecular Mechanisms to Therapeutic Strategies.
Restoring vision using optogenetics without being blind to the risks.
Caracterización clínico-epidemiológica en pacientes discapacitados visuales por retinosis pigmentaria. Sancti Spíritus. 2009-2019
A <i>Drosophila</i> Model Reveals the Potential Role for <i>mtt</i> in Retinal Disease.
Modeling autosomal dominant retinitis pigmentosa by using patient-specific retinal organoids with a class-3 RHO mutation.
<i>PRPH2</i>-Related Retinal Dystrophies: Mutational Spectrum in 103 Families from a Spanish Cohort.
Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants.
CRB1-associated retinal degeneration is dependent on bacterial translocation from the gut.
Emerging gene therapy products for RPGR-associated X-linked retinitis pigmentosa.
[Analysis of a patient with Retinitis pigmentosa due to a novel variant of IMPDH1 gene].