Chrome Extension
WeChat Mini Program
Use on ChatGLM
VIPCreated with Sketch.

Loss-of-function Variants in UBAP1L Cause Autosomal Recessive Retinal Degeneration.

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

Genetics in Medicine（2024）

Cited 4|Views41
Key words
Cone-rod dystrophy,Inherited retinal diseases,Rod-cone dystrophy,UBAP1L,Ubiquitin-associated protein 1-like
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined