Article info

Short report
The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype

Authors

  1. Correspondence to Professor Andrew T Hattersley, NIHR Clinical Research Facility, University of Exeter Medical School, Barrack Road, Exeter, Devon EX2 5DW, UK; a.t.hattersley{at}exeter.ac.uk
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Citation

Hamilton AJ, Bingham C, McDonald TJ, et al
The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype

Publication history

  • Received September 24, 2013
  • Revised October 22, 2013
  • Accepted October 23, 2013
  • First published November 27, 2013.
Online issue publication 
February 14, 2014

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