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
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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 -