[PDF][PDF] LRRK2 mutations and Parkinsonism
M Albrecht - The Lancet, 2005 - thelancet.com
The Lancet, 2005•thelancet.com
1 Nichols WC, Pankratz N, Hernandez D, et al. Genetic screening for a single common
LRRK2 mutation in familial Parkinson's disease. Lancet 2005; 365: 410–12. 2 DiFonzo A,
Rohe CF, Ferreira J, et al. A frequent LRRK2 gene mutation associated with autosomal
dominant Parkinson's disease. Lancet 2005; 365: 412–15. 3 Gilks WP, Abou-Sleiman PM,
Gandhi S, et al. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet 2005;
365: 415–16.
LRRK2 mutation in familial Parkinson's disease. Lancet 2005; 365: 410–12. 2 DiFonzo A,
Rohe CF, Ferreira J, et al. A frequent LRRK2 gene mutation associated with autosomal
dominant Parkinson's disease. Lancet 2005; 365: 412–15. 3 Gilks WP, Abou-Sleiman PM,
Gandhi S, et al. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet 2005;
365: 415–16.
1 Nichols WC, Pankratz N, Hernandez D, et al. Genetic screening for a single common LRRK2 mutation in familial Parkinson’s disease. Lancet 2005; 365: 410–12. 2 DiFonzo A, Rohe CF, Ferreira J, et al. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson’s disease. Lancet 2005; 365: 412–15. 3 Gilks WP, Abou-Sleiman PM, Gandhi S, et al. A common LRRK2 mutation in idiopathic Parkinson’s disease. Lancet 2005; 365: 415–16.
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