Associated Papers
Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.
Christodoulou K et al.
Gut, 2013
22543157 (PubMed )
Supplement: gutjnl-2011-301833-s1.pdf
A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients.
Shojaee S et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2009
The LRRK2 gene in Parkinson's disease: mutation screening in patients from Germany.
Schlitter AM et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2006
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