The R98Q variation in DJ-1 represents a rare polymorphism
- PMID: 14705128
- DOI: 10.1002/ana.10816
The R98Q variation in DJ-1 represents a rare polymorphism
Comment on
-
Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.Ann Neurol. 2003 Aug;54(2):271-4. doi: 10.1002/ana.10663. Ann Neurol. 2003. PMID: 12891685
Similar articles
-
DJ-1: the second gene for early onset Parkinson disease.Neurology. 2004 Feb 10;62(3):357-8. doi: 10.1212/wnl.62.3.357. Neurology. 2004. PMID: 14872011 No abstract available.
-
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.Mov Disord. 2004 Jul;19(7):796-800. doi: 10.1002/mds.20131. Mov Disord. 2004. PMID: 15254937
-
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.Neurology. 2004 Feb 10;62(3):389-94. doi: 10.1212/01.wnl.0000113022.51739.88. Neurology. 2004. PMID: 14872018
-
Rare genetic mutations shed light on the pathogenesis of Parkinson disease.J Clin Invest. 2003 Jan;111(2):145-51. doi: 10.1172/JCI17575. J Clin Invest. 2003. PMID: 12531866 Free PMC article. Review. No abstract available.
-
Impact of genetic analysis on Parkinson's disease research.Mov Disord. 2003 Sep;18 Suppl 6:S96-8. doi: 10.1002/mds.10569. Mov Disord. 2003. PMID: 14502662 Review.
Cited by
-
Mutations in DJ-1 are rare in familial Parkinson disease.Neurosci Lett. 2006 Nov 20;408(3):209-13. doi: 10.1016/j.neulet.2006.09.003. Epub 2006 Sep 25. Neurosci Lett. 2006. PMID: 16997464 Free PMC article.
-
DJ1 analysis in a large cohort of Italian early onset Parkinson Disease patients.Neurosci Lett. 2013 Dec 17;557 Pt B(PB):165-70. doi: 10.1016/j.neulet.2013.10.048. Epub 2013 Oct 28. Neurosci Lett. 2013. PMID: 24176883 Free PMC article.
-
High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's disease.J Mol Diagn. 2008 May;10(3):217-24. doi: 10.2353/jmoldx.2008.070100. Epub 2008 Apr 10. J Mol Diagn. 2008. PMID: 18403612 Free PMC article.
-
Mutation analysis of the seven in absentia homolog 1 (SIAH1) gene in Parkinson's disease.J Neural Transm (Vienna). 2006 Dec;113(12):1903-8. doi: 10.1007/s00702-006-0480-z. Epub 2006 Jun 6. J Neural Transm (Vienna). 2006. PMID: 16752048
-
Dissembled DJ-1 high molecular weight complex in cortex mitochondria from Parkinson's disease patients.Mol Neurodegener. 2009 Jun 4;4:23. doi: 10.1186/1750-1326-4-23. Mol Neurodegener. 2009. PMID: 19497122 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous