Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomalies

Human Genetics 2026 Open access

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Authors: Adeline Jacquinet, Lydie C. Flasse, Manon Dohet, Romane Vanhaeren, Hélène Pendeville, Carol A. Saunders, Anna Lehman, Catherine Pienkowski, Karine Morcel, D. J. Guerrier, Vincent Bours, Bernard Peers
DOI: 10.1007/s00439-025-02806-1
Cited by: 1
References: 78

Fields of Study & Subjects

Nuclear Receptors and Signaling Fetal and Pediatric Neurological Disorders Cancer-related Molecular Pathways

Publication details

Journal / source
Human Genetics
Publisher
Springer Science and Business Media LLC
Volume
145
Issue
1
Publication date
24 February 2026
Language
EN