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

Long-Read Sequencing to Unravel Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss

Giulia Ascari,Nanna D. Rendtorff,Marieke De Bruyne,Julie De Zaeytijd,Michel Van Lint,Mattias Van Heetvelde,Gavin Arno,Julie Jacob,David Creytens,Jo Van Dorpe,Thalia Van Laethem,Toon Rosseel,Tim De Pooter,Peter De Rijk,Wouter De Coster,Bjorn Menten,Alfredo Duenas Rey,Mojca Strazisar,Mette Bertelsen,Lisbeth Tranebjaerg,Elfride De Baere

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

Cited 10|Views40
Key words
CEP78,inherited retinal disease,cone-rod dystrophy with hearing loss,long-read sequencing,structural variants,single-cell gene expression analysis
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