Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases.

Summary

This is a publication. If there is no link to the publication on this page, you can try the pre-formated search via the search engines listed on this page.

Authors: Zeinab Fadaie; Laura Whelan; Tamar Ben-Yosef; Adrian Dockery; Zelia Corradi; Christian Gilissen; Lonneke Haer-Wigman; Jordi Corominas; Galuh D.N. Astuti; Galuh D.N. Astuti; Laura de Rooij; L. Ingeborgh van den Born; Caroline C W Klaver; Caroline C W Klaver; Carel B. Hoyng; Niamh Wynne; Emma Duignan; Paul F. Kenna; Paul F. Kenna; Frans P.M. Cremers; G. Jane Farrar; Susanne Roosing

Journal title: NPJ Genomic Medicine, 6

Journal number: 1

Journal publisher: Genomic medicine

Published year: 2021

DOI identifier: 10.1038/s41525-021-00261-1

ISSN: 2056-7944