Concepedia

Publication | Open Access

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

292

Citations

18

References

2010

Year

Abstract

This large series showed that the severity of the renal disease associated with HNF1B mutations was extremely variable (from prenatal renal failure to normal renal function in adulthood) and was not correlated with the genotype.

References

YearCitations

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