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

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 ; 14(10): e1007748, 2018 10.

Article em En | MEDLINE | ID: mdl-30365502

ABSTRACT

ABSTRACT

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

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2018 Tipo de documento: Article

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google