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A novel mutation in ATP13A2 gene in a patient with complicated hereditary spastic paraplegia accompanied by tubulopathy.
Inan, Berin; Azman, Filiz; Aktas, Dilek; Yildiz, Yilmaz; Saygi, Serap.
Afiliação
  • Inan B; Department of Neurology, Hacettepe University Faculty of Medicine, 06100, Sihhiye, Ankara, Turkey. berin.inan@yahoo.com.
  • Azman F; Department of Neurology, Hacettepe University Faculty of Medicine, 06100, Sihhiye, Ankara, Turkey.
  • Aktas D; Damagen Genetic Diagnostic Center, Ankara, Turkey.
  • Yildiz Y; Division of Pediatric Metabolism, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Saygi S; Department of Neurology, Hacettepe University Faculty of Medicine, 06100, Sihhiye, Ankara, Turkey.
Acta Neurol Belg ; 123(5): 1985-1987, 2023 10.
Article em En | MEDLINE | ID: mdl-35789476
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária Idioma: En Ano de publicação: 2023 Tipo de documento: Article