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Novel valosin-containing protein mutations associated with multisystem proteinopathy.
Al-Tahan, Sejad; Al-Obeidi, Ebaa; Yoshioka, Hiroshi; Lakatos, Anita; Weiss, Lan; Grafe, Marjorie; Palmio, Johanna; Wicklund, Matt; Harati, Yadollah; Omizo, Molly; Udd, Bjarne; Kimonis, Virginia.
Afiliação
  • Al-Tahan S; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, CA.
  • Al-Obeidi E; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, CA.
  • Yoshioka H; Department of Radiological Sciences, University of California, Irvine, CA.
  • Lakatos A; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, CA.
  • Weiss L; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, CA.
  • Grafe M; Department of Pathology, Oregon Health and Science University, Portland, OR.
  • Palmio J; Neuromuscular Research Center, Tampere University and University Hospital, Neurology, Tampere, Finland.
  • Wicklund M; Department of Neurology, University of Colorado School of Medicine, Aurora, CO.
  • Harati Y; Department of Neurology, Baylor College of Medicine, Houston, TX.
  • Omizo M; Deschutes Osteoporosis Center, Bend, OR.
  • Udd B; Neuromuscular Research Center, Tampere University and University Hospital, Neurology, Tampere, Finland; Folkhälsan Institute of Genetics and the Department of Medical Genetics, Haartman Institute, University of Helsinki, Helsinki, Finland; Neurology Department, Vasa Central Hospital, Vasa, Finland.
  • Kimonis V; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, CA. Electronic address: vkimonis@uci.edu.
Neuromuscul Disord ; 28(6): 491-501, 2018 06.
Article em En | MEDLINE | ID: mdl-29754758
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteíte Deformante / Doença de Parkinson / Mutação de Sentido Incorreto / Proteína com Valosina / Esclerose Lateral Amiotrófica / Doenças Musculares Tipo de estudo: Risk_factors_studies Limite: Adult / Aged / Humans / Male / Middle aged Idioma: En Revista: Neuromuscul Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteíte Deformante / Doença de Parkinson / Mutação de Sentido Incorreto / Proteína com Valosina / Esclerose Lateral Amiotrófica / Doenças Musculares Tipo de estudo: Risk_factors_studies Limite: Adult / Aged / Humans / Male / Middle aged Idioma: En Revista: Neuromuscul Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá