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Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.
Wortmann, Saskia B; Zietkiewicz, Szymon; Guerrero-Castillo, Sergio; Feichtinger, René G; Wagner, Matias; Russell, Jacqui; Ellaway, Carolyn; Mróz, Dagmara; Wyszkowski, Hubert; Weis, Denisa; Hannibal, Iris; von Stülpnagel, Celina; Cabrera-Orefice, Alfredo; Lichter-Konecki, Uta; Gaesser, Jenna; Windreich, Randy; Myers, Kasiani C; Lorsbach, Robert; Dale, Russell C; Gersting, Søren; Prada, Carlos E; Christodoulou, John; Wolf, Nicole I; Venselaar, Hanka; Mayr, Johannes A; Wevers, Ron A.
Afiliação
  • Wortmann SB; University Children's Hospital, Paracelsus Medical University (PMU), Salzburg, Austria. s.wortmann@salk.at.
  • Zietkiewicz S; Radboud Center for Mitochondrial Medicine, Department of Pediatrics, Amalia Children's Hospital, Radboudumc, Nijmegen, The Netherlands. s.wortmann@salk.at.
  • Guerrero-Castillo S; United for Metabolic Diseases (UMD), Amsterdam, The Netherlands. s.wortmann@salk.at.
  • Feichtinger RG; Intercollegiate Faculty of Biotechnology, University of Gdansk, Gdansk, Poland.
  • Wagner M; University Children's Research@Kinder-UKE, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Russell J; University Children's Hospital, Paracelsus Medical University (PMU), Salzburg, Austria.
  • Ellaway C; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg, Germany.
  • Mróz D; Institute of Human Genetics, Technical University of Munich, Munich, Germany.
  • Wyszkowski H; Genetic Metabolic Disorders Service, Sydney Children's Hospital Network, Randwick, NSW, Australia.
  • Weis D; Genetic Metabolic Disorders Service, Sydney Children's Hospital Network, Randwick, NSW, Australia.
  • Hannibal I; Discipline of Child & Adolescent Health; Sydney Medical School, University of Sydney, Sydney, NSW, Australia.
  • von Stülpnagel C; Discipline of Genetic Medicine, Sydney Medical School, University of Sydney, Sydney, NSW, Australia.
  • Cabrera-Orefice A; Intercollegiate Faculty of Biotechnology, University of Gdansk, Gdansk, Poland.
  • Lichter-Konecki U; Intercollegiate Faculty of Biotechnology, University of Gdansk, Gdansk, Poland.
  • Gaesser J; Department of Medical Genetics, Med Campus IV, Kepler University Hospital, Johannes Kepler University, Linz, Austria.
  • Windreich R; Division of Pediatric Neurology, Developmental Medicine and Social Pediatrics, Department of Pediatrics, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, Munich, Germany.
  • Myers KC; Division of Pediatric Neurology, Developmental Medicine and Social Pediatrics, Department of Pediatrics, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, Munich, Germany.
  • Lorsbach R; Institute for Transition, Rehabilitation and Palliation, Paracelsus Medical University, Salzburg, Austria.
  • Dale RC; Center for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences (RIMLS), Nijmegen, The Netherlands.
  • Gersting S; Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
  • Prada CE; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Christodoulou J; Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
  • Wolf NI; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Venselaar H; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Mayr JA; Division of Blood and Marrow Transplantation and Cellular Therapies, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
  • Wevers RA; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Genet Med ; 23(9): 1789, 2021 Sep.
Article em En | MEDLINE | ID: mdl-34302123

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Áustria
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