Titre:
  • The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease.
Auteur:Metzger, Silke; Bauer, Peter; Tomiuk, Juergen; Laccone, Franco; Didonato, Stefano; Gellera, Cinzia; Soliveri, Paola; Lange, Herwig W; Weirich-Schwaiger, Helga; Wenning, Gregor K; Melegh, Bela; Havasi, Victoria; Balikó, Lazlo; Wieczorek, Stefan; Arning, Larissa; Zaremba, Jacek; Sulek, Anna; Hoffman-Zacharska, Dorota; Basak, A Nazli; Ersoy, Nagehan; Zidovska, Jana; Kebrdlova, Vera; Pandolfo, Massimo; Ribaï, Pascale; Kadasi, Ludovit; Kvasnicova, Marta; Weber, Bernhard H F; Kreuz, Friedmar; Dose, Matthias; Stuhrmann, Manfred; Riess, Olaf
Informations sur la publication:Neurogenetics, 7, 1, page (27-30)
Statut de publication:Publié, 2006-03
Sujet CREF:Sciences bio-médicales et agricoles
MeSH keywords:Age of Onset
Humans
Huntington Disease -- genetics
Huntington Disease -- physiopathology
Nerve Tissue Proteins -- genetics
Nuclear Proteins -- genetics
Polymorphism, Genetic
Trinucleotide Repeats
Ubiquitin Thiolesterase -- genetics
Note générale:Journal Article
Research Support, Non-U.S. Gov't
SCOPUS: ar.j
Langue:Anglais
Identificateurs:urn:issn:1364-6745
info:doi/10.1007/s10048-005-0023-z
info:scp/33644658207
info:pmid/16369839