Mutations in the Hepatocyte Nuclear Factor-1β Gene Are Associated with Familial Hypoplastic Glomerulocystic Kidney Disease

Similar Items

• The mutated human gene encoding hepatocyte nuclear factor 1β inhibits kidney formation in developing Xenopus embryos
  od: Wild, Wiltrud, i dr.
  Izdano: (2000)
• Mutations in hepatocyte nuclear factor‐1β and their related phenotypes
  od: Edghill, E L, i dr.
  Izdano: (2006)
• Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic
  od: Clissold, Rhian L, i dr.
  Izdano: (2018)
• RET gene mutations are not a common cause of congenital solitary functioning kidney in adults
  od: Oram, Richard A., i dr.
  Izdano: (2009)
• Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic Testing
  od: Clissold, Rhian, i dr.
  Izdano: (2015)