Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration-Reference-Cited by-同舟云学术

Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration

Published:2024-06 Issue:6 Volume:26 Page:101106
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Han Ji Hoon^ORCID,Rodenburg Kim^ORCID,Hayman Tamar^ORCID,Calzetti Giacomo^ORCID,Kaminska Karolina^ORCID,Quinodoz Mathieu^ORCID,Marra Molly^ORCID,Wallerich Sandrine,Allon Gilad,Nagy Zoltán Z.,Knézy Krisztina,Li Yumei^ORCID,Chen Rui^ORCID,Barboni Mirella Telles Salgueiro^ORCID,Yang Paul,Pennesi Mark E.^ORCID,van den Born L. Ingeborgh^ORCID,Varsányi Balázs^ORCID,Szabó Viktória,Sharon Dror^ORCID,Banin Eyal,Ben-Yosef Tamar,Roosing Susanne^ORCID,Koenekoop Robert K.,Rivolta Carlo^ORCID

Publisher

Elsevier BV

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2. Advances in Ubiquitination and Proteostasis in Retinal Degeneration;Frontiers in Bioscience-Landmark;2024-07-22

3. Molecular Mechanisms Governing Sight Loss in Inherited Cone Disorders;Genes;2024-06-01