Skip Navigation

Corrigendum for Kabuta et al., Hum. Mol. Genet. 17 (10) 1482-1496.


Human Molecular Genetics Advance Access published online on May 26, 2008
Human Molecular Genetics, doi:10.1093/hmg/ddn155
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
17/14/2255    most recent
ddn155v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Kabuta, T.
Right arrow Articles by Wada, K.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Kabuta, T.
Right arrow Articles by Wada, K.
Social Bookmarking
Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2008. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Aberrant molecular properties shared by familial Parkinson's disease-associated mutant UCH-L1 and carbonyl-modified UCH-L1

Tomohiro Kabuta, Rieko Setsuie, Takeshi Mitsui, Aiko Kinugawa, Mikako Sakurai, Shunsuke Aoki, Kenko Uchida and Keiji Wada

The first 10% of the full text of this article appears below.

Human Molecular Genetics, 17; . . . [Full Text of this Article]


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?