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Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation.
De Michele, Giovanna; Galatolo, Daniele; Lieto, Maria; Fico, Tommasina; Saccà, Francesco; Santorelli, Filippo M; Filla, Alessandro.
Afiliación
  • De Michele G; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
  • Galatolo D; Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Fondazione Stella Maris, Pisa, Italy.
  • Lieto M; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
  • Fico T; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
  • Saccà F; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
  • Santorelli FM; Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Fondazione Stella Maris, Pisa, Italy.
  • Filla A; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy. Electronic address: afilla@unina.it.
Parkinsonism Relat Disord ; 76: 42-43, 2020 07.
Article en En | MEDLINE | ID: mdl-32559632
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ataxia / ATPasas de Translocación de Protón / Trastornos Parkinsonianos / Mioclonía Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Aged / Humans / Male Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Italia
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ataxia / ATPasas de Translocación de Protón / Trastornos Parkinsonianos / Mioclonía Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Aged / Humans / Male Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Italia