Related Experiment Video
Updated: Jul 23, 2025

Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo
Published on: September 22, 2017
Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy
Sylvie Gerber1, Lola Lessard2, Cécile Rouzier3,4
1IHU Imagine - Institut des Maladies Génétiques, Laboratoire de Génétique Ophtalmologique (LGO), Université Paris Descartes, Paris, France.
Abstract:
Gerber et al report 2 autosomal recessive pathogenic Misato homolog 1 (MSTO1) variants causing hereditary optic atrophy and raise concerns about a previously identified dominant variant of MSTO1 by Gal et al (2017).
More Related Videos
09:34Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
09:37Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
Published on: August 15, 2019
Related Concept Videos
Genetic Lingo
The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
Photoreceptors and Visual Pathways
Glaucoma: Overview
Pleiotropy
Translation
Translation Produces the Building Blocks of Life
Proteins are...