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Parkinson's disease in GTP cyclohydrolase 1 mutation carriers International Parkinson's Disease Genomics Consortium, UCL-exomes consortium 2014
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A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation Le Gal, Francois; Korff, Christian; Monso-Hinard, Christine; Mund, Michael T.; ... Schmitt-Mechelke, Thomas 2010
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Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry Benjamin, Emelia J.; Ehret, Georg Benedikt 2009
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Early stimulation of DYT1 primary generalized dystonia prevents from its secondary irreversible complications Anheim, Mathieu; Vercueil, Laurent; Fraix, Valerie; Chabardes, Stephan; ... Pollak, Pierre 2008