Zobrazeno 1 - 10
of 502
pro vyhledávání: '"Sb, Dunnett"'
Autor:
Andreas Heuer, L. A. Jones, Zubeyde Bayram-Weston, SB Dunnett, Gemma Higgs, Narinder Janghra, Simon Philip Brooks
Publikováno v:
Clinical Genetics. 76:76-84
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 85:A25-A26
Background Huntington’s disease (HD) is a genetic disorder caused by a mutation of the huntingtin gene (HTT) resulting in an expanded polyglutamine (CAG) repeat length in the mutant huntingtin protein (mHTT). The mutation induces a progressive dysf
Publikováno v:
Europe PubMed Central
Autor:
Marc Peschanski, SB Dunnett
Publikováno v:
The Lancet Neurology. 1:81
Publikováno v:
Europe PubMed Central
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ce80d019f560b96b30b8b5fd9a0f42da
http://europepmc.org/abstract/med/3073422
http://europepmc.org/abstract/med/3073422
Autor:
Orth M, Oj, Handley, Schwenke C, Sb, Dunnett, Craufurd D, Ak, Ho, Wild E, Sj, Tabrizi, Georg Bernhard Landwehrmeyer, Disease Network, Investigators Of The European Huntington S.
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::02625a7e3e1071e730c2f454b3b10b0c
http://europepmc.org/abstract/med/20890398
http://europepmc.org/abstract/med/20890398
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9f82426d2fbd82022f0fd3aab9e199c8
http://www.scopus.com/inward/record.url?eid=2-s2.0-0021955180&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0021955180&partnerID=MN8TOARS
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::07bd3fb03c78bb96b4a725f317ea5cb7
http://europepmc.org/abstract/med/2857778
http://europepmc.org/abstract/med/2857778