| 1 | DCTN1, PERS |
| DCTN1 mutations are implicated in multiple neurodegenerative disorders. | |
| Uribe V. | |
| Clin Genet 77(1):32-4. No abstract available. PMID: 20101786 2010 | |
| 2 | DCTN1, PERS |
| DCTN1 mutations in Perry syndrome. | |
| Farrer MJ, Hulihan MM, Kachergus JM, Dächsel JC, Stoessl AJ, Grantier LL, Calne S, Calne DB, Lechevalier B, Chapon F, Tsuboi Y, Yamada T, Gutmann L, Elibol B, Bhatia KP, Wider C, Vilariño-Güell C, Ross OA, Brown LA, Castanedes-Casey M, Dickson DW, Wszolek ZK. | |
| Nat Genet 41(2):163-5. Epub 2009 Jan 11. 2009 | |
| 3 | PERS |
| Japanese family with parkinsonism, depression, weight loss, and central hypoventilation. | |
| Tsuboi Y, Wszolek ZK, Kusuhara T, Doh-ura K, Yamada T. | |
| Neurology 58(7):1025-30. 2002 | |