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A novel mutation of RASA1 in capillary malformation-arteriovenous malformation syndrome in a case with spinal cord involvement.
Moreno-Estébanez, Ana; Losada Domingo, Jose María; Catalli, Claudio; González-Pinto González, Tirso; Agirre-Beitia, Garazi; Campos Rodríguez, Iria; Díaz-Cuervo, Irene; Lasa Elgezua, Olatz.
Afiliação
  • Moreno-Estébanez A; Neurology Department, Cruces University Hospital, Plaza Cruces SN 48903, Barakaldo, Basque Country, Spain. Electronic address: ana.morenoestebanez@osakidetza.eus.
  • Losada Domingo JM; Neurology Department, Cruces University Hospital, Plaza Cruces SN 48903, Barakaldo, Basque Country, Spain.
  • Catalli C; Genetics Department, Cruces University Hospital, Plaza Cruces SN 48903, Barakaldo, Basque Country, Spain.
  • González-Pinto González T; Neurology Department, Cruces University Hospital, Plaza Cruces SN 48903, Barakaldo, Basque Country, Spain.
  • Agirre-Beitia G; Neurology Department, Cruces University Hospital, Plaza Cruces SN 48903, Barakaldo, Basque Country, Spain.
  • Campos Rodríguez I; Neurology Department, Cruces University Hospital, Plaza Cruces SN 48903, Barakaldo, Basque Country, Spain.
  • Díaz-Cuervo I; Neurology Department, Cruces University Hospital, Plaza Cruces SN 48903, Barakaldo, Basque Country, Spain.
  • Lasa Elgezua O; Dermatology Department, Cruces University Hospital, Plaza Cruces SN 48903, Barakaldo, Basque Country, Spain.
Clin Neurol Neurosurg ; 195: 105965, 2020 08.
Article em En | MEDLINE | ID: mdl-32485551

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Malformações Arteriovenosas / Medula Espinal / Capilares / Mancha Vinho do Porto / Proteína p120 Ativadora de GTPase / Mutação Limite: Adult / Humans / Male Idioma: En Revista: Clin Neurol Neurosurg Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Malformações Arteriovenosas / Medula Espinal / Capilares / Mancha Vinho do Porto / Proteína p120 Ativadora de GTPase / Mutação Limite: Adult / Humans / Male Idioma: En Revista: Clin Neurol Neurosurg Ano de publicação: 2020 Tipo de documento: Article