The genetics of Parkinson disease: to test or not to test
- PMID: 17803021
- DOI: 10.1017/s0317167100006661
The genetics of Parkinson disease: to test or not to test
Comment on
-
LRRK2 is not a significant cause of Parkinson's disease in French-Canadians.Can J Neurol Sci. 2007 Aug;34(3):333-5. doi: 10.1017/s0317167100006776. Can J Neurol Sci. 2007. PMID: 17803032
-
LRRK2 screening in a Canadian Parkinson's disease cohort.Can J Neurol Sci. 2007 Aug;34(3):336-8. doi: 10.1017/s0317167100006788. Can J Neurol Sci. 2007. PMID: 17803033
Similar articles
-
Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations.Neurology. 2008 Jul 22;71(4):303; author reply 303-4. doi: 10.1212/01.wnl.0000320511.30222.dd. Neurology. 2008. PMID: 18645174 No abstract available.
-
Test for LRRK2 mutations in patients with Parkinson's disease.Pract Neurol. 2008 Dec;8(6):381-5. doi: 10.1136/jnnp.2008.162420. Pract Neurol. 2008. PMID: 19015299
-
LRRK2: both a cause and a risk factor for Parkinson disease?Neurology. 2005 Sep 13;65(5):664-5. doi: 10.1212/01.wnl.0000179342.58181.c9. Neurology. 2005. PMID: 16157895 No abstract available.
-
[Genetics and present therapy options in Parkinson's disease: a review].Ideggyogy Sz. 2009 May 30;62(5-6):155-63. Ideggyogy Sz. 2009. PMID: 19579663 Review. Hungarian.
-
[Parkinson disease: genetics and neuronal death].Rev Neurol (Paris). 2009 Apr;165 Spec No 2:F80-5. Rev Neurol (Paris). 2009. PMID: 19593875 Review. French. No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical