A Novel NPTX1 de novo Variant in a Late-Onset Ataxia Patient.

Deppe, Jonas; Deininger, Natalie; Lingor, Paul; Haack, Tobias B; Haslinger, Bernhard; Deschauer, Marcus

Deppe, Jonas; Deininger, Natalie; Lingor, Paul; Haack, Tobias B; Haslinger, Bernhard; Deschauer, Marcus.

Afiliação

Deppe J; Department of Neurology, School of Medicine, Technical University of Munich, Munich, Germany.
Deininger N; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Lingor P; Department of Neurology, School of Medicine, Technical University of Munich, Munich, Germany.
Haack TB; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Haslinger B; Centre for Rare Diseases, University of Tübingen, Tübingen, Germany.
Deschauer M; Department of Neurology, School of Medicine, Technical University of Munich, Munich, Germany.

Mov Disord ; 37(6): 1319-1321, 2022 06.

Article em En | MEDLINE | ID: mdl-35285082

Assuntos

Ataxia Cerebelar; Ataxia/genética; Humanos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia Cerebelar Limite: Humans Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha

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