Variable phenotype in HNF1B mutations: Extrarenal manifestations distinguish affected individuals from the population with congenital anomalies of the kidney and urinary tract

  1. Madariaga, L.
  2. García-Castaño, A.
  3. Ariceta, G.
  4. Martínez-Salazar, R.
  5. Aguayo, A.
  6. Castaño, L.
Aldizkaria:
Clinical Kidney Journal

ISSN: 2048-8513,  2048-8505

Argitalpen urtea: 2019

Alea: 12

Zenbakia: 3

Orrialdeak: 373-379

Mota: Artikulua

DOI: 10.1093/CKJ/SFY102 GOOGLE SCHOLAR lock_openSarbide irekia editor

Garapen Iraunkorreko Helburuak

Datuen iturria: Scopus