A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.

Bademci G, Edwards TL, Torres AL, Scott WK, Z├╝chner S, Martin ER, Vance JM, Wang L
Hum Mutat. 2010 31 (10): E1767-71

PMID: 20809526 · PMCID: PMC3025121 · DOI:10.1002/humu.21351

MeSH Terms (10)

Age of Onset Female Gene Deletion Gene Dosage Genome-Wide Association Study Humans Middle Aged Parkinson Disease Polymorphism, Single Nucleotide Tyrosine 3-Monooxygenase

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