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Correction: A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells.
Awamleh, Zain; Choufani, Sanaa; Wu, Wendy; Rots, Dmitrijs; Dingemans, Alexander J M; Nadif Kasri, Nael; Boronat, Susana; Ibañez-Mico, Salvador; Cuesta Herraiz, Laura; Ferrer, Irene; Martínez Carrascal, Antonio; Pérez-Jurado, Luis A; Aznar Lain, Gemma; Ortigoza-Escobar, Juan Dario; de Vries, Bert B A; Koolen, David A; Weksberg, Rosanna.
Afiliação
  • Awamleh Z; Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada.
  • Choufani S; Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada.
  • Wu W; Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada.
  • Rots D; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands.
  • Dingemans AJM; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands.
  • Nadif Kasri N; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands.
  • Boronat S; Department of Pediatrics, Hospital del Santa Creu y Sant Pau, Barcelona, Spain.
  • Ibañez-Mico S; Department of Pediatric Neurology, Hospital Virgen de la Arrixaca, Murcia, Madrid, Spain.
  • Cuesta Herraiz L; Department of Pediatric Neurology, Hospital de Manises, Valencia, Spain.
  • Ferrer I; Department of Genetics, Consorcio Hospital General de Valencia, Valencia, Spain.
  • Martínez Carrascal A; Department of Pediatrics, Hospital de Requena, Valencia, Spain.
  • Pérez-Jurado LA; Genetics Unit, Universitat Pompeu Fabra, Hospital del Mar Research Institute (IMIM) and CIBERER, Barcelona, Spain.
  • Aznar Lain G; Genetics Unit, Universitat Pompeu Fabra, Hospital del Mar Research Institute (IMIM) and CIBERER, Barcelona, Spain.
  • Ortigoza-Escobar JD; Movement Disorders Unit, Institut de Recerca Sant Joan de Déu, CIBERER-ISCIII and European Reference Network for Rare Neurological Diseases (ERN-RND), Barcelona, Spain.
  • de Vries BBA; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands.
  • Koolen DA; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands. david.koolen@radboudumc.nl.
  • Weksberg R; Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada. rweksb@sickkids.ca.
Eur J Hum Genet ; 32(3): 366, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38355964
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Eur J Hum Genet Ano de publicação: 2024 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Eur J Hum Genet Ano de publicação: 2024 Tipo de documento: Article