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Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ ‐ 1 (T497C) genes in familial Parkinson's disease from the Gene PD study
Parkinson's disease (PD) is a neurodegenerative disorder in which relatives of the probands are affected approximately 4 times as frequently as relatives of control subjects. Several genes have been implicated as genetic risk factors for PD. We investigated the presence of six reported genetic...
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Published in: | Movement disorders 2005-09, Vol.20 (9), p.1188-1191 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Parkinson's disease (PD) is a neurodegenerative disorder in which relatives of the probands are affected approximately 4 times as frequently as relatives of control subjects. Several genes have been implicated as genetic risk factors for PD. We investigated the presence of six reported genetic variations in the
SCNA
,
NR4A2
, and
DJ
‐
1
genes in 292 cases of familial Parkinson's disease from the
Gene
PD study. None of the variants were found in the
Gene
PD families. Our results suggest that other variants or genes account for the familial risk of PD within the
Gene
PD study. © 2005 Movement Disorder Society |
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ISSN: | 0885-3185 1531-8257 |
DOI: | 10.1002/mds.20515 |