Spectrum of HNF1B Mutations in a Large Cohort of Patients Who Harbor Renal Diseases

Background and objectives: Hepatocyte nuclear factor 1β (HNF1β) is a transcription factor that is critical for the development of kidney and pancreas. In humans, mutations in HNF1B lead to congenital anomalies of the kidney and urinary tract, pancreas atrophy, and maturity-onset diabetes of the youn...

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Bibliografische gegevens
Hoofdauteurs: Heidet, Laurence, Decramer, Stéphane, Pawtowski, Audrey, Morinière, Vincent, Bandin, Flavio, Knebelmann, Bertrand, Lebre, Anne-Sophie, Faguer, Stanislas, Guigonis, Vincent, Antignac, Corinne, Salomon, Rémi
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society of Nephrology 2010
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Original Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2879303/
https://ncbi.nlm.nih.gov/pubmed/20378641
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.06810909
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