دورية أكاديمية
أعرض في EDS

Corrigendum: Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort.

التفاصيل البيبلوغرافية
العنوان: Corrigendum: Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort.
المؤلفون: Leman R; Laboratoire de Biologie Clinique et Oncologique, Centre François Baclesse, 14000 Caen, France.; Inserm U1245 Genomics and Personalized Medecine in Cancer and Neurological Disorders, Normandie Univ, UNIROUEN, Normandy Centre for Genomic and Personalized Medicine, 76031 Rouen, France.; Normandie Univ, UNICAEN, 14000 Caen, France., Gaildrat P; Inserm U1245 Genomics and Personalized Medecine in Cancer and Neurological Disorders, Normandie Univ, UNIROUEN, Normandy Centre for Genomic and Personalized Medicine, 76031 Rouen, France., Gac GL; Inserm UMR1078, Genetics, Functional Genomics and Biotechnology, Université de Bretagne Occidentale, 29200 Brest, France., Ka C; Inserm UMR1078, Genetics, Functional Genomics and Biotechnology, Université de Bretagne Occidentale, 29200 Brest, France., Fichou Y; Inserm UMR1078, Genetics, Functional Genomics and Biotechnology, Université de Bretagne Occidentale, 29200 Brest, France., Audrezet MP; Inserm UMR1078, Genetics, Functional Genomics and Biotechnology, Université de Bretagne Occidentale, 29200 Brest, France., Caux-Moncoutier V; Inserm U830, Institut Curie Centre de Recherches, 75005 Paris, France.; Université Paris Descartes, Sorbonne Paris Cité, 75005 Paris, France.; Service de Génétique, Institut Curie, 75005 Paris, France., Caputo SM; Service de Génétique, Institut Curie, 75005 Paris, France., Boutry-Kryza N; Unité Mixte de Génétique Constitutionnelle des Cancers Fréquents, Hospices Civils de Lyon, 69000 Lyon, France., Léone M; Unité Mixte de Génétique Constitutionnelle des Cancers Fréquents, Hospices Civils de Lyon, 69000 Lyon, France., Mazoyer S; Lyon Neuroscience Research Center-CRNL, Inserm U1028, CNRS UMR 5292, University of Lyon, 69008 Lyon, France., Bonnet-Dorion F; Inserm U916, Département de Pathologie, Laboratoire de Génétique Constitutionnelle, Institut Bergonié, 33000 Bordeaux, France., Sevenet N; Inserm U916, Département de Pathologie, Laboratoire de Génétique Constitutionnelle, Institut Bergonié, 33000 Bordeaux, France., Guillaud-Bataille M; Gustave Roussy, Université Paris-Saclay, Département de Biopathologie, 94805 Villejuif, France., Rouleau E; Gustave Roussy, Université Paris-Saclay, Département de Biopathologie, 94805 Villejuif, France., Paillerets BB; Gustave Roussy, Université Paris-Saclay, Département de Biopathologie, 94805 Villejuif, France., Wappenschmidt B; Division of Molecular Gynaeco-Oncology, Department of Gynaecology and Obstetrics, University Hospital of Cologne, 50937 Cologne, Germany., Rossing M; Centre for Genomic Medicine, Rigshospitalet, University of Copenhagen, 1017 Copenhagen, Denmark., Muller D; Laboratoire d'Oncogénétique, Centre Paul Strauss, 67000 Strasbourg, France., Bourdon V; Laboratoire d'Oncogénétique Moléculaire, Institut Paoli-Calmettes, 13009 Marseille, France., Revillon F; Laboratoire d'Oncogénétique Moléculaire Humaine, Centre Oscar Lambret, 59000 Lille, France., Parsons MT; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, 4006 Herston, Queensland, Australia., Rousselin A; Laboratoire de Biologie Clinique et Oncologique, Centre François Baclesse, 14000 Caen, France.; Inserm U1245 Genomics and Personalized Medecine in Cancer and Neurological Disorders, Normandie Univ, UNIROUEN, Normandy Centre for Genomic and Personalized Medicine, 76031 Rouen, France., Davy G; Laboratoire de Biologie Clinique et Oncologique, Centre François Baclesse, 14000 Caen, France.; Inserm U1245 Genomics and Personalized Medecine in Cancer and Neurological Disorders, Normandie Univ, UNIROUEN, Normandy Centre for Genomic and Personalized Medicine, 76031 Rouen, France., Castelain G; Inserm U1245 Genomics and Personalized Medecine in Cancer and Neurological Disorders, Normandie Univ, UNIROUEN, Normandy Centre for Genomic and Personalized Medicine, 76031 Rouen, France., Castéra L; Laboratoire de Biologie Clinique et Oncologique, Centre François Baclesse, 14000 Caen, France.; Inserm U1245 Genomics and Personalized Medecine in Cancer and Neurological Disorders, Normandie Univ, UNIROUEN, Normandy Centre for Genomic and Personalized Medicine, 76031 Rouen, France., Sokolowska J; Service de Génétique, CHU Nancy, 54035 Nancy, France., Coulet F; Service de génétique, Hôpital Pitié Salpétrière, AP-HP, 75013 Paris, France., Delnatte C; Laboratoire de génétique moléculaire, CHU Nantes, 44000 Nantes, France., Férec C; Inserm UMR1078, Genetics, Functional Genomics and Biotechnology, Université de Bretagne Occidentale, 29200 Brest, France., Spurdle AB; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, 4006 Herston, Queensland, Australia., Martins A; Inserm U1245 Genomics and Personalized Medecine in Cancer and Neurological Disorders, Normandie Univ, UNIROUEN, Normandy Centre for Genomic and Personalized Medicine, 76031 Rouen, France., Krieger S; Laboratoire de Biologie Clinique et Oncologique, Centre François Baclesse, 14000 Caen, France.; Inserm U1245 Genomics and Personalized Medecine in Cancer and Neurological Disorders, Normandie Univ, UNIROUEN, Normandy Centre for Genomic and Personalized Medicine, 76031 Rouen, France.; Normandie Univ, UNICAEN, 14000 Caen, France., Houdayer C; Inserm U830, Institut Curie Centre de Recherches, 75005 Paris, France.; Université Paris Descartes, Sorbonne Paris Cité, 75005 Paris, France.; Service de Génétique, Institut Curie, 75005 Paris, France.
المصدر: Nucleic acids research [Nucleic Acids Res] 2018 Nov 30; Vol. 46 (21), pp. 11656-11657.
نوع المنشور: Journal Article; Published Erratum
اللغة: English
بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium: Internet ISSN: 1362-4962 (Electronic) Linking ISSN: 03051048 NLM ISO Abbreviation: Nucleic Acids Res Subsets: PubMed not MEDLINE
أسماء مطبوعة: Publication: 1992- : Oxford : Oxford University Press
Original Publication: London, Information Retrieval ltd.
التعليقات: Erratum for: Nucleic Acids Res. 2018 Sep 6;46(15):7913-7923. (PMID: 29750258)
تواريخ الأحداث: Date Created: 20181016 Latest Revision: 20191120
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC6277085
DOI: 10.1093/nar/gky979
PMID: 30321405
قاعدة البيانات: MEDLINE
الوصف
تدمد:1362-4962
DOI:10.1093/nar/gky979