LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century
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| Description | scientific article published in August 2005 |
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author: Suzanne Lesage French Parkinson's Disease Genetics Study Group Ebba Lohmann Anne-Louise Leutenegger Alexandra Durr Alexis Brice Sabine Janin Bs |
| Publication date | August 1, 2005 |
| Language | English |
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