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Original article
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum

Authors

  1. Correspondence to Professor Dr H Krude, Charité University Medicine Berlin, Institute for Experimental Pediatric Endocrinology, Augustenburger Platz 1, Berlin 13353, Germany; heiko.krude{at}charite.de Dr R Ullmann, Institut für Radiobiologie der Bundeswehr in Verbindung mit der Universität Ulm, D-80937 Munich, Germany; ullmann{at}molgen.mpg.de
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Citation

Thorwarth A, Schnittert-Hübener S, Schrumpf P, et al
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum

Publication history

  • Received December 23, 2013
  • Revised February 8, 2014
  • Accepted February 18, 2014
  • First published April 8, 2014.
Online issue publication 
May 17, 2014

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