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“Parkinson LRRK2” Clear search

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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

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.

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