Human Genome Epidemiology Literature Finder
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Query Trace: Parkinson Disease and TH[original query] |
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A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease. Human mutation 2010 Oct 31 (10): E1767-71. Bademci Güney, Edwards Todd L, Torres Andre L, Scott William K, Züchner Stephan, Martin Eden R, Vance Jeffery M, Wang Liyo |
- Page last reviewed:Feb 1, 2024
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