| 1 | HTRA2, PARK13 |
| Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease. | |
| Chao YX, Ng EY, Foo JN, Liu J, Zhao Y, Tan EK. | |
| Neurogenetics 16(3):241-2. doi: 10.1007/s10048-015-0443-3. Epub 2015 Mar 20. No abstract available. 2015 | |
| 2 | HTRA2, PARK13 |
| Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls. | |
| Simon-Sanchez J, Singleton AB. | |
| Hum Mol Genet 17(13):1988-93. Epub 2008 Mar 25. 2008 | |
| 3 | HTRA2, PARK13 |
| 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, MŸller T, Bornemann A, Wolburg H, Downward J, Riess O, Schulz JB, KrŸger R. | |
| Hum Mol Genet 14(15):2099-111. Epub 2005 Jun 16. 2005 | |