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Genetic screening for a single common LRRK2 mutation in f... | ResearchHub
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Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
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Authors
William Nichols
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William Nichols
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Nathan Pankratz
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Tatiana Foroud
Published
January 1, 2005
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Journal
The Lancet
Topics
Biology
Internal Medicine
Medicine
Neurology
Cellular And Molecular Neuroscience
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DOI
10.1016/s0140-6736(05)17828-3
