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Paper Details

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation.
Sci Adv
20
2021
ARID1A, ARID1A/B, HCF1, LINKED (LINKage-specific deubiquitylation deficiency-induced Embryonic Defects) syndrome, OTUD5, chromatin, congenital anomalies, deubiquitylase, histone deacetylase 2, human, multiple, neuroectodermal enhancers, patients, ubiquitin
Author NameAffiliation
Joann BodurthaJohns Hopkins Hospital
Ellen MacnamaraNational Human Genome Research Institute, National Institutes of Health
Cynthia J TifftOffice of the Clinical Director, National Human Genome Research Institute, National Institutes of Health
Cynthia J TifftNational Human Genome Research Institute, National Institutes of Health
Cynthia J TifftOffice of the Clinical Director, National Human Genome Research Institute, National Institutes of Health
Cynthia J TifftNational Human Genome Research Institute, National Institutes of Health
Daniel L KastnerNational Human Genome Research Institute, National Institutes of Health
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