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PDFCopy-number variation
Original article
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum
- 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
Citation
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
September 22, 2016
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