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author 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
de Villemeur, Thierry Billette
Nava, Caroline
Afenjar, Alexandra
Keren, Boris
Bodmer, Rolf
Antignac, Corinne
Simons, Matias
author_facet 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
de Villemeur, Thierry Billette
Nava, Caroline
Afenjar, Alexandra
Keren, Boris
Bodmer, Rolf
Antignac, Corinne
Simons, Matias
author_sort Gonçalves, Sara
collection PubMed
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spelling pubmed-62034102018-11-19 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 de Villemeur, Thierry Billette Nava, Caroline Afenjar, Alexandra Keren, Boris Bodmer, Rolf Antignac, Corinne Simons, Matias PLoS Genet Correction Public Library of Science 2018-10-26 /pmc/articles/PMC6203410/ /pubmed/30365502 http://dx.doi.org/10.1371/journal.pgen.1007748 Text en © 2018 Gonçalves et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Correction
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
de Villemeur, Thierry Billette
Nava, Caroline
Afenjar, Alexandra
Keren, Boris
Bodmer, Rolf
Antignac, Corinne
Simons, Matias
Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies
title Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies
title_full Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies
title_fullStr Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies
title_full_unstemmed Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies
title_short Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies
title_sort correction: a homozygous kat2b variant modulates the clinical phenotype of add3 deficiency in humans and flies
topic Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203410/
https://www.ncbi.nlm.nih.gov/pubmed/30365502
http://dx.doi.org/10.1371/journal.pgen.1007748
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