Association of rare <i>apolipoprotein E</i> ε4 homozygosity with an earlier age at onset in spinocerebellar ataxia type 3
Charlotte Clara Meyer(University of Tübingen), Thorsten Schmidt(University of Tübingen), Gunnar Blumenstock(University of Tübingen), Laura Bannach Jardim(Universidade Federal do Rio Grande do Sul), B van de Warrenburg, Priscila Pereira Sena(University of Tübingen), Sylvie Forlani(Centre National de la Recherche Scientifique), P. Bauer(Centogene (Germany)), Sylvia Boesch(Innsbruck Medical University), Heike Jacobi(Heidelberg University), Eduardo Preusser de Mattos(Universidade Federal do Rio Grande do Sul), A. Brice(Centre National de la Recherche Scientifique), Carlos R. Gordon(Tel Aviv University), A. Durr(Centre National de la Recherche Scientifique), Sandra Szymanski(St. Josef-Hospital), Tanja Schmitz-Hübsch, Marcondes Cavalcante França(Universidade Estadual de Campinas (UNICAMP)), Paola Giunti, Dagmar Timmann, Maria-Luiza Saraiva-Pereira(Universidade Federal do Rio Grande do Sul), Rahel Maria Burger(University of Tübingen), Ludger Schöls(German Center for Neurodegenerative Diseases), Jörg B Schulz, Massimo Pandolfo, Bart P van de Warrenburg(Radboud University Nijmegen), Thomas Klockgether(German Center for Neurodegenerative Diseases), Mario R Cornejo-Olivas(Universidad Científica del Sur), José Berciano, Bela Melegh, Sophie Tezenas du Montcel, Olaf Riess(University of Tübingen), Giovanni Stévanin(Inserm), The EUROSCA Network, Roy Zaltzman(Tel Aviv University)
Cited by 1
Related Papers
Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis
|The Lancet Neurology|2004|1.1k
Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders
|Science|2014|548
The natural history of multiple system atrophy: a prospective European cohort study
|The Lancet Neurology|2013|533
Transgenic rat model of Huntington's disease
|Human Molecular Genetics|2003|349
Inflammatory reactions and severe neutropenia in mice lacking the transcriptional repressor Gfi1
|Nature Genetics|2002|319