Associated Papers
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.
Zheng B et al.
American Journal of Medical Genetics. Part A, 2022
A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling.
Vivante A et al.
Journal of the American Society of Nephrology : Jasn, 2017
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