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Browsing by Author Durr, A.

Full Text	Issue Date	Title	Author(s)
	2010	Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.	Vermeer, S.; Hoischen, A.; Meijer, R.P., et al
	2011	A two-stage meta-analysis identifies several new loci for Parkinson's disease.	Plagnol, V.; Nalls, M.A.; Bras, J.M., et al
	2012	Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease	Keller, M.F.; Saad, M.; Bras, J., et al
	2010	Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.	Schulz, J.B.; Borkert, J.; Wolf, S., et al