Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.
Strauss, Karsten M.; Martins, L. Miguel; Plun-Favreau, Helene; Marx, Frank P.; Kautzmann, Sabine; Berg, Daniela; Gasser, Thomas; Wszolek, Zbginiew; Müller, Thomas; Bornemann, Antje; Wolburg, Hartwig; Downward, Julian; Riess, Olaf; Schulz, Jörg B.; Krüger, Rejko; Human Molecular Genetics, 2005, vol. 14, issue 15, p 2099, ISSN 09646906. ISBN 09646906.

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