Variable phenotype in HNF1B mutations: extrarenal manifestations distinguish affected individuals from the population with congenital anomalies of the kidney and urinary tract
Resumen
Palabras clave
CAKUT; HNF1B; MODY
Citación recomendada
Madariaga L, García-Castaño A, Ariceta G, Martínez-Salazar R, Aguayo A, Castaño L, et al. Variable phenotype in HNF1B mutations: extrarenal manifestations distinguish affected individuals from the population with congenital anomalies of the kidney and urinary tract. Clin Kidney J. 2019;12(3):373–9.
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https://hdl.handle.net/11351/4231Este elemento aparece en las siguientes colecciones
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