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UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration.
Fahed, Akl C; McDonough, Barbara; Gouvion, Cynthia M; Newell, Kathy L; Dure, Leon S; Bebin, Martina; Bick, Alexander G; Seidman, J G; Harter, Donald H; Seidman, Christine E.
Afiliação
  • Fahed AC; Department of Genetics, Harvard Medical School, Boston, MA.
  • McDonough B; Department of Genetics, Harvard Medical School, Boston, MA.
  • Gouvion CM; Cardiovascular Division and Howard Hughes Medical Institute, Brigham and Women's Hospital, Boston, MA.
  • Newell KL; Departments of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS.
  • Dure LS; Departments of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS.
  • Bebin M; Departments of Neurology and Pediatrics, University of Alabama at Birmingham, Birmingham, AL.
  • Bick AG; Departments of Neurology and Pediatrics, University of Alabama at Birmingham, Birmingham, AL.
  • Seidman JG; Department of Genetics, Harvard Medical School, Boston, MA.
  • Harter DH; Department of Genetics, Harvard Medical School, Boston, MA.
  • Seidman CE; Department of Neurology, School of Medicine & Health Sciences, The George Washington University, Washington, DC.
Ann Neurol ; 75(5): 793-798, 2014 May.
Article em En | MEDLINE | ID: mdl-24771548
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ubiquitinas / Heterogeneidade Genética / Proteínas de Ciclo Celular / Transtornos Heredodegenerativos do Sistema Nervoso / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Aged / Child, preschool / Female / Humans / Male Idioma: En Revista: Ann Neurol Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Marrocos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ubiquitinas / Heterogeneidade Genética / Proteínas de Ciclo Celular / Transtornos Heredodegenerativos do Sistema Nervoso / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Aged / Child, preschool / Female / Humans / Male Idioma: En Revista: Ann Neurol Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Marrocos