G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients
Identifieur interne : 000D06 ( Istex/Checkpoint ); précédent : 000D05; suivant : 000D07G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients
Auteurs : H Deng [États-Unis] ; W Le [États-Unis] ; X Zhang [États-Unis] ; T Pan [États-Unis] ; J Jankovic [États-Unis]Source :
- Acta Neurologica Scandinavica [ 0001-6314 ] ; 2005-06.
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Abstract
Objective – To determine whether the G309D and W437OPA mutations in PINK1 gene are present in American Caucasian population of patients with Parkinson's disease (PD). Methods – We searched for the G309D and W437OPA mutation by sequencing the regions of interest in the PINK1 gene in 237 unrelated Caucasian patients. Results – None of the 237 samples showed the G309D or W437OPA mutations. Conclusions – The G309D and W437OPA mutations in PINK1 gene probably do not represent common causes of familial or sporadic PD in a Caucasian population.
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DOI: 10.1111/j.1600-0404.2005.00383.x
Affiliations:
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ISTEX:7454C0DB6D7A9A8C21D4D4C54E1484E8BA4B5342Le document en format XML
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<front><div type="abstract" xml:lang="en">Objective – To determine whether the G309D and W437OPA mutations in PINK1 gene are present in American Caucasian population of patients with Parkinson's disease (PD). Methods – We searched for the G309D and W437OPA mutation by sequencing the regions of interest in the PINK1 gene in 237 unrelated Caucasian patients. Results – None of the 237 samples showed the G309D or W437OPA mutations. Conclusions – The G309D and W437OPA mutations in PINK1 gene probably do not represent common causes of familial or sporadic PD in a Caucasian population.</div>
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