SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROME.

Date publication

juin 2026

Journal

American journal of ophthalmology

Auteurs

Membres identifiés du Cancéropôle Est :
Dr HERAULT Yann

Tous les auteurs :
Moshiri A, Kasiri N, Shea M, Ali L, Yang B, Shao A, Clary D, Flenniken AM, Eskandarian M, Amarie OV, Becker L, Sangermano R, Place EM, Bujakowska KM, Huckfeldt RM, Berberovic Z, Bour R, Riet F, Brown SD, D'Souza A, Fuchs H, Gailus-Durner V, Guimond A, Hérault Y, de Angelis MH, Lux A, Mittelhauser C, Nutter LMJ, Palkova M, Lindovsky J, Petit-Demouliere B, Prochazka J, Bradaschia V, Kelsey L, McKerlie C, Raishbrook MJ, Sedlacek R, ,Lanoue L, Lloyd KK, Roux MJ, Bermingham-McDonogh O

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/42309414

Résumé

The purpose of this project was to identify novel Usher syndrome (USH) candidate genes from phenotyping data of 9,139 knockout (KO) mouse lines.

Mots clés

Auditory abnormality, Dual sensory impairment, Knockout mouse, Retinal abnormality, Usher syndrome, genetic variants

Référence

Am J Ophthalmol. 2026 06 17;: