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A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.
Lorefice, L; Tranquilli, S; Fenu, G; Murru, M R; Frau, J; Rolesu, M; Coghe, G C; Marrosu, F; Marrosu, M G; Cocco, E.
Afiliação
  • Lorefice L; Department of Public Health and Clinical and Molecular Medicine, Multiple Sclerosis Center, University of Cagliari, Ospedale "Binaghi", via Is Guadazzonis, 2, 09126, Cagliari, Italy. lorena.lorefice@hotmail.it.
  • Tranquilli S; Department of Medical Sciences, Institute of Neurology, University of Cagliari, Cagliari, Italy.
  • Fenu G; Department of Public Health and Clinical and Molecular Medicine, Multiple Sclerosis Center, University of Cagliari, Ospedale "Binaghi", via Is Guadazzonis, 2, 09126, Cagliari, Italy.
  • Murru MR; ASL8-Department of Medical Sciences, Multiple Sclerosis Center, University of Cagliari, Cagliari, Italy.
  • Frau J; Department of Public Health and Clinical and Molecular Medicine, Multiple Sclerosis Center, University of Cagliari, Ospedale "Binaghi", via Is Guadazzonis, 2, 09126, Cagliari, Italy.
  • Rolesu M; ASL8-Department of Medical Sciences, Multiple Sclerosis Center, University of Cagliari, Cagliari, Italy.
  • Coghe GC; Department of Public Health and Clinical and Molecular Medicine, Multiple Sclerosis Center, University of Cagliari, Ospedale "Binaghi", via Is Guadazzonis, 2, 09126, Cagliari, Italy.
  • Marrosu F; Department of Medical Sciences, Institute of Neurology, University of Cagliari, Cagliari, Italy.
  • Marrosu MG; Department of Medical Sciences, Multiple Sclerosis Center, University of Cagliari, Cagliari, Italy.
  • Cocco E; Department of Public Health and Clinical and Molecular Medicine, Multiple Sclerosis Center, University of Cagliari, Ospedale "Binaghi", via Is Guadazzonis, 2, 09126, Cagliari, Italy.
Neurol Sci ; 36(12): 2213-20, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26194536
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia / Tremor / Expansão das Repetições de Trinucleotídeos / Proteína do X Frágil da Deficiência Intelectual / Síndrome do Cromossomo X Frágil / Esclerose Múltipla / Mutação Tipo de estudo: Diagnostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Neurol Sci 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: Ataxia / Tremor / Expansão das Repetições de Trinucleotídeos / Proteína do X Frágil da Deficiência Intelectual / Síndrome do Cromossomo X Frágil / Esclerose Múltipla / Mutação Tipo de estudo: Diagnostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Neurol Sci Ano de publicação: 2015 Tipo de documento: Article