A141s - and - g399s mutation in the omi / htra2 - protein in parkinson's disease

摘要

Nucleic acid molecule encoding a human omi / htra2 - protein, the at amino acid 141 and / or 399 a with respect to the wild type genetic modification, as well as for the corresponding sections thereof, for use in the diagnosis of parkinson''s disease and / or a disposition to it and / or for finding and testing of substances which are active against parkinson''s disease.