Age of onset in Huntington's disease is influenced by CAG repeat variations in other polyglutamine disease-associated genes.

Stuitje, Geerte; van Belzen, Martine J; Gardiner, Sarah L; van Roon-Mom, Willeke M C; Boogaard, Merel W; Tabrizi, Sarah J; Roos, Raymund A C; Aziz, N A

Stuitje, Geerte; van Belzen, Martine J; Gardiner, Sarah L; van Roon-Mom, Willeke M C; Boogaard, Merel W; Tabrizi, Sarah J; Roos, Raymund A C; Aziz, N A.

Afiliação

Stuitje G; Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands.
van Belzen MJ; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Gardiner SL; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
van Roon-Mom WMC; Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands.
Boogaard MW; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Tabrizi SJ; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Aziz NA; Department of Neurodegenerative Disease, UCL Huntington's Disease Centre, University College London Institute of Neurology, London, UK.

Brain ; 140(7): e42, 2017 07 01.

Article em En | MEDLINE | ID: mdl-28549075

Assuntos

Doença de Huntington; Ataxias Espinocerebelares; Humanos; Peptídeos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Huntington / Ataxias Espinocerebelares Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Brain Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda

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