PUBLICATION
Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomalies
- Authors
- Jacquinet, A., Flasse, L., Dohet, M., Vanhaeren, R., Pendeville, H., Saunders, C., Lehman, A., Pienkowski, C., Morcel, K., Guerrier, D., Bours, V., Peers, B.
- ID
- ZDB-PUB-260225-4
- Date
- 2026
- Source
- Human genetics 145: (Journal)
- Registered Authors
- Peers, Bernard, Pendeville-Samain, Hélène
- Keywords
- CRISPR-Cas9 zebrafish model, Costovertebral defects, NR6A1 variants, Nr6a1a and nr6a1b, Renal agenesis, Uterine anomalies
- MeSH Terms
- none
- PubMed
- 41733738 Full text @ Hum. Genet.
Citation
Jacquinet, A., Flasse, L., Dohet, M., Vanhaeren, R., Pendeville, H., Saunders, C., Lehman, A., Pienkowski, C., Morcel, K., Guerrier, D., Bours, V., Peers, B. (2026) Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomalies. Human genetics. 145:.
Abstract
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping