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Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder.
Lossos, Alexander; Elazar, Nimrod; Lerer, Israela; Schueler-Furman, Ora; Fellig, Yakov; Glick, Benjamin; Zimmerman, Bat-El; Azulay, Haim; Dotan, Shlomo; Goldberg, Sharon; Gomori, John M; Ponger, Penina; Newman, J P; Marreed, Hodaifah; Steck, Andreas J; Schaeren-Wiemers, Nicole; Mor, Nofar; Harel, Michal; Geiger, Tamar; Eshed-Eisenbach, Yael; Meiner, Vardiella; Peles, Elior.
Afiliação
  • Lossos A; 1 Department of Neurology and Agnes Ginges Centre for Human Neurogenetics, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel vmeiner@hadassah.org.il also@hadassah.org.il peles@weizmann.ac.il.
  • Elazar N; 2 Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
  • Lerer I; 3 Department of Genetics and Metabolic Diseases, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
  • Schueler-Furman O; 4 Department of Microbiology and Molecular Genetics, Institute for Medical Research Israel-Canada, Faculty of Medicine, Hebrew University, Jerusalem, Israel.
  • Fellig Y; 5 Department of Pathology, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
  • Glick B; 6 Paediatric Neuromuscular Service, Alyn Paediatric Rehabilitation Centre, Jerusalem, Israel.
  • Zimmerman BE; 3 Department of Genetics and Metabolic Diseases, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
  • Azulay H; 5 Department of Pathology, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
  • Dotan S; 7 Department of Ophthalmology, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
  • Goldberg S; 7 Department of Ophthalmology, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
  • Gomori JM; 8 Department of Radiology, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
  • Ponger P; 1 Department of Neurology and Agnes Ginges Centre for Human Neurogenetics, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
  • Newman JP; 1 Department of Neurology and Agnes Ginges Centre for Human Neurogenetics, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
  • Marreed H; 3 Department of Genetics and Metabolic Diseases, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel.
  • Steck AJ; 9 Department of Biomedicine, University Hospital Basel, University of Basel, Switzerland.
  • Schaeren-Wiemers N; 9 Department of Biomedicine, University Hospital Basel, University of Basel, Switzerland.
  • Mor N; 2 Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
  • Harel M; 10 Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Geiger T; 10 Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Eshed-Eisenbach Y; 2 Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
  • Meiner V; 3 Department of Genetics and Metabolic Diseases, Hebrew University-Hadassah Medical Centre, Jerusalem, Israel vmeiner@hadassah.org.il also@hadassah.org.il peles@weizmann.ac.il.
  • Peles E; 2 Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Brain ; 138(Pt 9): 2521-36, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26179919
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicoproteína Associada a Mielina / Doença de Pelizaeus-Merzbacher / Mutação Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Brain Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicoproteína Associada a Mielina / Doença de Pelizaeus-Merzbacher / Mutação Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Brain Ano de publicação: 2015 Tipo de documento: Article