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Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients.
Urreizti, Roser; Mayer, Klaus; Evrony, Gilad D; Said, Edith; Castilla-Vallmanya, Laura; Cody, Neal A L; Plasencia, Guillem; Gelb, Bruce D; Grinberg, Daniel; Brinkmann, Ulrich; Webb, Bryn D; Balcells, Susanna.
Afiliação
  • Urreizti R; Department of Genetics, Microbiology and Statistics, Faculty of Biology, University of Barcelona, IBUB, IRSJD, CIBERER, Barcelona, Spain. roseruf@yahoo.es.
  • Mayer K; Roche Pharma Research and Early Development. Large Molecule Research, Roche Innovation Center, Munich, Nonnenwald 2, 82377, Penzberg, Germany.
  • Evrony GD; Center for Human Genetics and Genomics, New York University Langone Health, New York, NY, USA.
  • Said E; Section of Medical Genetics, Mater dei Hospital, Msida, Malta.
  • Castilla-Vallmanya L; Department of Anatomy and Cell Biology, University of Malta, Msida, Malta.
  • Cody NAL; Department of Genetics, Microbiology and Statistics, Faculty of Biology, University of Barcelona, IBUB, IRSJD, CIBERER, Barcelona, Spain.
  • Plasencia G; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Gelb BD; Sema4, Stamford, CT, USA.
  • Grinberg D; Lead Molecular Design, S.L, Sant Cugat del Vallés, Spain.
  • Brinkmann U; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Webb BD; Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Balcells S; Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Eur J Hum Genet ; 28(1): 138, 2020 Jan.
Article em En | MEDLINE | ID: mdl-31477843
Following the publication of the article, it was noted that the last column in Table 1, the total % should have read 5/8 (62.5) for the 'Epilepsy' row, and not 5.7 (71.4). This has now been amended in the HTML and PDF of the original article.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article