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Paper Details

Integrated genome and transcriptome analyses reveal the mechanism of genome instability in ataxia with oculomotor apraxia 2.
Proc Natl Acad Sci U S A
14
2022
ALS4, AOA2, Cockayne syndrome, Cockayne syndrome protein CSB, GCskew, R, RAD52, Senataxin, XPF, XPG, amyotrophic lateral sclerosis 4, ataxia with, ataxia with oculomotor apraxia 2, chromosomal regions, chromosome, chromosome fragile sites, genes, genome, human, mouse, oculomotor apraxia 2, patient, patient-derived cells, progressive neurodegenerative diseases, promoter-proximal regions, promoters, transcription-coupled repair endonucleases
Author NameAffiliation
Richard MitterThe Francis Crick Institute
Amnon KorenCornell University
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Release 1.2