Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209)

Diana Braunholz, Melanie Hullings, María Concepcion Gil-Rodríguez, Christopher T. Fincher, Mark B. Mallozzi, Elizabeth Loy, Melanie Albrecht, Maninder Kaur, Janusz Limon, Abhinav Rampuria, Dinah Clark, Antonie Kline, Andreas Dalski, Juliane Eckhold, Andreas Tzschach, Raoul Hennekam, Gabriele Gillessen-Kaesbach, Jolanta Wierzba, Ian D. Krantz, Matthew A. DeardorffFrank J. Kaiser

Research output: Contribution to journalComment/debate

Original languageEnglish (US)
Number of pages1
JournalEuropean Journal of Human Genetics
Volume20
Issue number3
DOIs
StatePublished - Mar 1 2012
Externally publishedYes

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Braunholz, D., Hullings, M., Gil-Rodríguez, M. C., Fincher, C. T., Mallozzi, M. B., Loy, E., Albrecht, M., Kaur, M., Limon, J., Rampuria, A., Clark, D., Kline, A., Dalski, A., Eckhold, J., Tzschach, A., Hennekam, R., Gillessen-Kaesbach, G., Wierzba, J., Krantz, I. D., ... Kaiser, F. J. (2012). Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209). European Journal of Human Genetics, 20(3). https://doi.org/10.1038/ejhg.2011.209