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2016
Mark Deletions at 22q11.2 in idiopathic Parkinson's disease : a combined analysis of genome-wide association data
Mok, Kin Y ; Sheerin, Una ; Simón-Sánchez, Javier ; Salaka, Afnan ; Chester, Lucy ; Escott-Price, Valentina ; Mantripragada, Kiran ; Doherty, Karen M ; Noyce, Alastair J and Mencacci, Niccolo E , et al. (2016) In The Lancet Neurology 15(6). p.96-585
- Contribution to journal › Article
Mark A genome-wide association study in multiple system atrophy
Sailer, Anna ; Scholz, Sonja W. ; Nalls, Michael A. ; Schulte, Claudia ; Federoff, Monica ; Price, T. Ryan ; Lees, Andrew ; Ross, Owen A. ; Dickson, Dennis W. and Mok, Kin , et al. (2016) In Neurology 87(15). p.1591-1598
- Contribution to journal › Article
2012
Mark Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.
Englund, Elisabet ^LU ; Gustafson, Lars ^LU ; Passant, Ulla ^LU ; Majounie, Elisa ; Renton, Alan E ; Traynor, Bryan J ; Rohrer, Jonathan D ; Mok, Kin and Hardy, John (2012) In Neurobiology of Aging
- Contribution to journal › Article
Mark Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Majounie, Elisa ; Renton, Alan E. ; Mok, Kin ; Dopper, Elise G. P. ; Waite, Adrian ; Rollinson, Sara ; Chio, Adrian ; Restagno, Gabriella ; Nicolaou, Nayia and Simon-Sanchez, Javier , et al. (2012) In Lancet Neurology 11(4). p.323-330
- Contribution to journal › Article