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Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.

Strauss KM, Martins LM, Plun-Favreau H, Marx FP, Kautzmann S, Berg D, Gasser T, Wszolek Z, Muller T, Bornemann A, Wolburg H, Downward J, Riess O, Schulz JB, Kruger R
Hum Mol Genet. 2005 Aug 1. 14(15):2099-111. (Link opens in a new window) PubMed (Link opens in a new window) Article

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