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Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's diseaseWINKLER, Susan; KÖNIG, Inke R; LOHMANN-HEDRICH, Katja et al.European journal of human genetics. 2007, Vol 15, Num 11, pp 1163-1168, issn 1018-4813, 6 p.Article

Autosomal Dominant Myoclonus-Dystonia and Tourette Syndrome in a Family Without Linkage to the SGCE GeneORTH, Michael; DJARMATI, Ana; BÄUMER, Tobias et al.Movement disorders. 2007, Vol 22, Num 14, pp 2090-2096, issn 0885-3185, 7 p.Article

Childhood-onset Restless Legs Syndrome : Clinical and Genetic Features of 22 FamiliesMUHLE, Hiltrud; NEUMANN, Anja; STEPHANI, Ulrich et al.Movement disorders. 2008, Vol 23, Num 8, pp 1113-1121, issn 0885-3185, 9 p.Article

Myoclonus-Dystonia Due to Maternal Uniparental DisomyGUETTARD, Emilie; PORTNOI, Marie-France; KLEIN, Christine et al.Archives of neurology (Chicago). 2008, Vol 65, Num 10, pp 1380-1385, issn 0003-9942, 6 p.Article

Biological effects of the PINK1 c.1366C>T mutation : implications in Parkinson disease pathogenesisGRÜNEWALD, Anne; BREEDVELD, Guido J; LESAGE, Suzanne et al.Neurogenetics (Oxford. Print). 2007, Vol 8, Num 2, pp 103-109, issn 1364-6745, 7 p.Article

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