SCIENTIFIC LITERATURE · MED

Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's disease.

Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Rudolph A, Shults CW, Foroud T, Nichols WC, Parkinson Study Group-PROGENI Investigators.

Mov Disord · 2006-12-01

DOI: 10.1002/mds.21162PMID: 17078063

Check source for accessComparative Study; Journal Article; Research Support, N.I.H., ExtramuralOriginal source ↗

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