Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Anja Schrewed"'
Autor:
Sabine M Hölter, Mary Stromberg, Marina Kovalenko, Lillian Garrett, Lisa Glasl, Edith Lopez, Jolene Guide, Alexander Götz, Wolfgang Hans, Lore Becker, Birgit Rathkolb, Jan Rozman, Anja Schrewed, Martin Klingenspor, Thomas Klopstock, Holger Schulz, Eckhard Wolf, Wolfgang Wursta, Tammy Gillis, Hiroko Wakimoto, Jonathan Seidman, Marcy E MacDonald, Susan Cotman, Valérie Gailus-Durner, Helmut Fuchs, Martin Hrabě de Angelis, Jong-Min Lee, Vanessa C Wheeler
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e80923 (2013)
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by the expansion of a CAG trinucleotide repeat in the HTT gene encoding huntingtin. The disease has an insidious course, typically progressing over 10-15 years until
Externí odkaz:
https://doaj.org/article/57b263b8d55c4fe881fd6b6ee0978b4a
Autor:
Martin Klingenspor, Wolfgang Hans, Jolene R. Guide, Tammy Gillis, Jonathan G. Seidman, Lore Becker, Lisa Glasl, Susan L. Cotman, Sabine M. Hölter, Martin Hrabě de Angelis, Vanessa C. Wheeler, Jan Rozman, Lillian Garrett, Holger Schulz, Hiroko Wakimoto, Marcy E. MacDonald, Jong-Min Lee, Thomas Klopstock, Marina Kovalenko, Helmut Fuchs, Edith Lopez, Anja Schrewed, Wolfgang Wursta, Eckhard Wolf, Valerie Gailus-Durner, Birgit Rathkolb, Alexander Götz, Mary Stromberg
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e80923 (2013)
PLoS ONE 8:e80923 (2013)
PLOS ONE 8(11), e80923 (2013). doi:10.1371/journal.pone.0080923
PLoS ONE
PLoS ONE 8:e80923 (2013)
PLOS ONE 8(11), e80923 (2013). doi:10.1371/journal.pone.0080923
PLoS ONE
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder caused by the expansion of a CAG trinucleotide repeat in the HTT gene encoding huntingtin. The disease has an insidious course, typically progressing over 10-15 years unt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7a72eecfc1ec8da2fc0f5ff671c665c
https://doi.org/10.1371/journal.pone.0080923
https://doi.org/10.1371/journal.pone.0080923