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. Deardorff; Frank J. Kaiser

doi:10.1038/ejhg.2011.209

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

^*Corresponding author for this work

Institute of Human Genetics

Abstract

Since the publication of this article, the authors noted that NIPBL was mistyped in several places. This has now been rectified and the corrected article appears in this issue. The HTML and online PDF versions have also been rectified and now carry the correct name.

The authors would like to apologise for any inconvenience caused.

Original language	English
Journal	European Journal of Human Genetics
Volume	20
Issue number	3
Number of pages	1
ISSN	1018-4813
DOIs	https://doi.org/10.1038/ejhg.2011.209
Publication status	Published - 01.03.2012

Research Areas and Centers

Research Area: Medical Genetics

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1038/ejhg.2011.209

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

@article{9e67f14dc43e4dd086fe4c323e2657e4,

title = "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)",

abstract = "Since the publication of this article, the authors noted that NIPBL was mistyped in several places. This has now been rectified and the corrected article appears in this issue. The HTML and online PDF versions have also been rectified and now carry the correct name.The authors would like to apologise for any inconvenience caused.",

author = "Diana Braunholz and Melanie Hullings and Gil-Rodr{\'i}guez, {Mar{\'i}a Concepcion} and Fincher, {Christopher T.} and Mallozzi, {Mark B.} and Elizabeth Loy and Melanie Albrecht and Maninder Kaur and Janusz Limon and Abhinav Rampuria and Dinah Clark and Antonie Kline and Andreas Dalski and Juliane Eckhold and Andreas Tzschach and Raoul Hennekam and Gabriele Gillessen-Kaesbach and Jolanta Wierzba and Krantz, {Ian D.} and Deardorff, {Matthew A.} and Kaiser, {Frank J.}",

year = "2012",

month = mar,

day = "1",

doi = "10.1038/ejhg.2011.209",

language = "English",

volume = "20",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

number = "3",

}

Braunholz, D, Hullings, M, Gil-Rodríguez, MC, Fincher, CT, Mallozzi, MB, 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, ID, Deardorff, MA & Kaiser, FJ 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, vol. 20, no. 3. https://doi.org/10.1038/ejhg.2011.209

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). / Braunholz, Diana; Hullings, Melanie; Gil-Rodríguez, María Concepcion et al.
In: European Journal of Human Genetics, Vol. 20, No. 3, 01.03.2012.

Research output: Journal Articles › Comments/Debates

TY - JOUR

T1 - 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)

AU - Braunholz, Diana

AU - Hullings, Melanie

AU - Gil-Rodríguez, María Concepcion

AU - Fincher, Christopher T.

AU - Mallozzi, Mark B.

AU - Loy, Elizabeth

AU - Albrecht, Melanie

AU - Kaur, Maninder

AU - Limon, Janusz

AU - Rampuria, Abhinav

AU - Clark, Dinah

AU - Kline, Antonie

AU - Dalski, Andreas

AU - Eckhold, Juliane

AU - Tzschach, Andreas

AU - Hennekam, Raoul

AU - Gillessen-Kaesbach, Gabriele

AU - Wierzba, Jolanta

AU - Krantz, Ian D.

AU - Deardorff, Matthew A.

AU - Kaiser, Frank J.

PY - 2012/3/1

Y1 - 2012/3/1

N2 - Since the publication of this article, the authors noted that NIPBL was mistyped in several places. This has now been rectified and the corrected article appears in this issue. The HTML and online PDF versions have also been rectified and now carry the correct name.The authors would like to apologise for any inconvenience caused.

AB - Since the publication of this article, the authors noted that NIPBL was mistyped in several places. This has now been rectified and the corrected article appears in this issue. The HTML and online PDF versions have also been rectified and now carry the correct name.The authors would like to apologise for any inconvenience caused.

UR - http://www.scopus.com/inward/record.url?scp=84857164783&partnerID=8YFLogxK

U2 - 10.1038/ejhg.2011.209

DO - 10.1038/ejhg.2011.209

M3 - Comments/Debates

AN - SCOPUS:84857164783

SN - 1018-4813

VL - 20

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 3

ER -

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)

Abstract

Research Areas and Centers

UN SDGs

Access to Document

Other files and links

Fingerprint

Cite this