Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

William C Nichols1, Nathan Pankratz, Dena Hernandez

  • 1Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA. Bill.nichols@cchmc.org

Lancet (London, England)
|February 1, 2005
PubMed

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