SCIENTIFIC LITERATURE · MED

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century.

Lesage S, Leutenegger AL, Ibanez P, Janin S, Lohmann E, Dürr A, Brice A, French Parkinson's Disease Genetics Study Group.

Am J Hum Genet · 2005-08-01

DOI: 10.1086/432422PMID: 16145815

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