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Reply: Mutations in TUBB4A and spastic paraplegia.
Chamova, Teodora; Kancheva, Dahlia; Guergueltcheva, Velina; Mitev, Vanio; Azmanov, Dimitar N; Kalaydjieva, Luba; Jordanova, Albena; Tournev, Ivailo.
Afiliación
  • Chamova T; Medical University of Sofia, Faculty of Medicine, Department of Neurology, Clinic of Neurology, University Hospital Alexandrovska, Sofia, Bulgaria.
  • Kancheva D; Molecular Neurogenomics Group, Department of Molecular Genetics, Antwerp, Belgium.
  • Guergueltcheva V; Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.
  • Mitev V; Department of Medical Chemistry and Biochemistry, Molecular Medicine Center, Medical University-Sofia, Sofia, Bulgaria.
  • Azmanov DN; Department of Neurology, Sofiamed Hospital, Sofia, Bulgaria.
  • Kalaydjieva L; Department of Medical Chemistry and Biochemistry, Molecular Medicine Center, Medical University-Sofia, Sofia, Bulgaria.
  • Jordanova A; Department of Diagnostic Genomics, PathWest, QEII Medical Centre, Nedlands, WA, Australia.
  • Tournev I; Harry Perkins Institute of Medical Research and Centre for Medical Research, The University of Western Australia, Perth, Australia.
Mov Disord ; 30(13): 1858-9, 2015 Nov.
Article en En | MEDLINE | ID: mdl-26477690
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tubulina (Proteína) / Paraplejía Espástica Hereditaria / Genes Dominantes / Mosaicismo Límite: Female / Humans / Male Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Bulgaria
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tubulina (Proteína) / Paraplejía Espástica Hereditaria / Genes Dominantes / Mosaicismo Límite: Female / Humans / Male Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Bulgaria