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; Müller T; Bornemann A; Wolburg H; Downward J; Riess O; Schulz JB; Krüger R; Human Molecular Genetics, 2005, vol. 14, issue 15, p 2099, ISSN 09646906. ISBN 09646906.

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