Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Publication Date timeline is not available.
Page 1
Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system.
Ann Neurol. 2008 Apr;63(4):473-81. doi: 10.1002/ana.21328.
Ann Neurol. 2008.
PMID: 18306232
The mitochondrial 13513G > A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff-Parkinson-White.
Ruiter EM, Siers MH, van den Elzen C, van Engelen BG, Smeitink JA, Rodenburg RJ, Hol FA.
Ruiter EM, et al. Among authors: siers mh.
Eur J Hum Genet. 2007 Feb;15(2):155-61. doi: 10.1038/sj.ejhg.5201735. Epub 2006 Nov 15.
Eur J Hum Genet. 2007.
PMID: 17106447
Item in Clipboard
Exercise intolerance, muscle pain and lactic acidaemia associated with a 7497G>A mutation in the tRNASer(UCN) gene.
Grafakou O, Hol FA, Otfried Schwab K, Siers MH, ter Laak H, Trijbels F, Ensenauer R, Boelen C, Smeitink J.
Grafakou O, et al. Among authors: siers mh.
J Inherit Metab Dis. 2003;26(6):593-600. doi: 10.1023/a:1025960300710.
J Inherit Metab Dis. 2003.
PMID: 14605505
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.