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PRSS25

MIM.606441 2p12

Pathology

- loss of function germline mutation in Parkinson disease

See also

- serine proteases (PRSSs)

References

- 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, Schulz1 JB, Kruger R. Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson’s disease. Hum Mol Genet. 2005 Jun 16; PMID: 15961413