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Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies

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Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies. / Gonçalves, Sara; Patat, Julie; Guida, Maria Clara; Lachaussée, Noelle; Arrondel, Christelle; Helmstädter, Martin; Boyer, Olivia; Gribouval, Olivier; Gubler, Marie-Claire; Mollet, Geraldine; Rio, Marlène; Charbit, Marina; Bole-Feysot, Christine; Nitschke, Patrick; Huber, Tobias B; Wheeler, Patricia G; Haynes, Devon; Juusola, Jane; Villemeur, Thierry Billette de; Nava, Caroline; Afenjar, Alexandra; Keren, Boris; Bodmer, Rolf; Antignac, Corinne; Simons, Matias.

in: PLOS GENET, Jahrgang 14, Nr. 10, 10.2018, S. e1007748.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › Andere (Vorworte u.ä.) › Forschung

Harvard

Gonçalves, S, Patat, J, Guida, MC, Lachaussée, N, Arrondel, C, Helmstädter, M, Boyer, O, Gribouval, O, Gubler, M-C, Mollet, G, Rio, M, Charbit, M, Bole-Feysot, C, Nitschke, P, Huber, TB, Wheeler, PG, Haynes, D, Juusola, J, Villemeur, TBD, Nava, C, Afenjar, A, Keren, B, Bodmer, R, Antignac, C & Simons, M 2018, 'Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies', PLOS GENET, Jg. 14, Nr. 10, S. e1007748. https://doi.org/10.1371/journal.pgen.1007748

APA

Gonçalves, S., Patat, J., Guida, M. C., Lachaussée, N., Arrondel, C., Helmstädter, M., Boyer, O., Gribouval, O., Gubler, M-C., Mollet, G., Rio, M., Charbit, M., Bole-Feysot, C., Nitschke, P., Huber, T. B., Wheeler, P. G., Haynes, D., Juusola, J., Villemeur, T. B. D., ... Simons, M. (2018). Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies. PLOS GENET, 14(10), e1007748. https://doi.org/10.1371/journal.pgen.1007748

Vancouver

Gonçalves S, Patat J, Guida MC, Lachaussée N, Arrondel C, Helmstädter M et al. Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies. PLOS GENET. 2018 Okt;14(10):e1007748. https://doi.org/10.1371/journal.pgen.1007748

Bibtex

@article{54ca600e59644e0ba462deed48d36d8f,
title = "Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies",
abstract = "[This corrects the article DOI: 10.1371/journal.pgen.1007386.].",
keywords = "Published Erratum",
author = "Sara Gon{\c c}alves and Julie Patat and Guida, {Maria Clara} and Noelle Lachauss{\'e}e and Christelle Arrondel and Martin Helmst{\"a}dter and Olivia Boyer and Olivier Gribouval and Marie-Claire Gubler and Geraldine Mollet and Marl{\`e}ne Rio and Marina Charbit and Christine Bole-Feysot and Patrick Nitschke and Huber, {Tobias B} and Wheeler, {Patricia G} and Devon Haynes and Jane Juusola and Villemeur, {Thierry Billette de} and Caroline Nava and Alexandra Afenjar and Boris Keren and Rolf Bodmer and Corinne Antignac and Matias Simons",
note = "Document Type: Correction",
year = "2018",
month = oct,
doi = "10.1371/journal.pgen.1007748",
language = "English",
volume = "14",
pages = "e1007748",
journal = "PLOS GENET",
issn = "1553-7404",
publisher = "Public Library of Science",
number = "10",

}

RIS

TY - JOUR

T1 - Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies

AU - Gonçalves, Sara

AU - Patat, Julie

AU - Guida, Maria Clara

AU - Lachaussée, Noelle

AU - Arrondel, Christelle

AU - Helmstädter, Martin

AU - Boyer, Olivia

AU - Gribouval, Olivier

AU - Gubler, Marie-Claire

AU - Mollet, Geraldine

AU - Rio, Marlène

AU - Charbit, Marina

AU - Bole-Feysot, Christine

AU - Nitschke, Patrick

AU - Huber, Tobias B

AU - Wheeler, Patricia G

AU - Haynes, Devon

AU - Juusola, Jane

AU - Villemeur, Thierry Billette de

AU - Nava, Caroline

AU - Afenjar, Alexandra

AU - Keren, Boris

AU - Bodmer, Rolf

AU - Antignac, Corinne

AU - Simons, Matias

N1 - Document Type: Correction

PY - 2018/10

Y1 - 2018/10

N2 - [This corrects the article DOI: 10.1371/journal.pgen.1007386.].

AB - [This corrects the article DOI: 10.1371/journal.pgen.1007386.].

KW - Published Erratum

U2 - 10.1371/journal.pgen.1007748

DO - 10.1371/journal.pgen.1007748

M3 - Other (editorial matter etc.)

C2 - 30365502

VL - 14

SP - e1007748

JO - PLOS GENET

JF - PLOS GENET

SN - 1553-7404

IS - 10

ER -