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Paper Details

Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe.
Hum Mutat
23
2012
51 exons, Arg1628Pro, LRRK2, LRRK2 gene, LRRK2 mutations, PD, Parkinson disease, ROC, c4883G, c4883G>C, clinically, drug target genes, exonic variants, p, p.Arg1628Pro, person, single-nucleotide variants

Datasets

Release 1.2