Diagnostic exome sequencing in early‐onset Parkinson's disease confirms VPS13C as a rare cause of autosomal‐recessive Parkinson's disease.
Saved in:
| Title: | Diagnostic exome sequencing in early‐onset Parkinson's disease confirms VPS13C as a rare cause of autosomal‐recessive Parkinson's disease. |
|---|---|
| Authors: | Schormair, B.1,2, Kemlink, D.3, Mollenhauer, B.4,5, Fiala, O.3,6, Machetanz, G.4, Roth, J.3, Berutti, R.7, Strom, T. M.2,7, Haslinger, B.8, Trenkwalder, C.4, Zahorakova, D.9, Martasek, P.9, Ruzicka, E.3, Winkelmann, J.1,2,8,10 juliane.winkelmann@tum.de |
| Source: | Clinical Genetics. Mar2018, Vol. 93 Issue 3, p603-612. 11p. 1 Diagram, 8 Charts. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 00099163 |
|---|---|
| DOI: | 10.1111/cge.13124 |