| Property | Value |
|---|
| Working Groups |  Winkelmann |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  28862745 |
| DOI |  10.1111/cge.13124 |
| Publication Year | 2018 |
| Title | Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease.  |
| Journal | Clinical genetics |
| ISSN | 0009-9163 |
| ESSN | 1399-0004 |
| URL | https://www.ncbi.nlm.nih.gov/pubmed/?term=28862745%5Buid%5D |
| Pages | 603-612 |
| Issue | 3 |
| Volume | 93 |
| Journal Abbreviation | Clin Genet |
| Authors | Schormair B, Kemlink D, Mollenhauer B, Fiala O, Machetanz G, Roth J, Berutti R, Strom TM, Haslinger B, Trenkwalder C, Zahorakova D, Martasek P, Ruzicka E, Winkelmann J |
| First Author | Schormair B |
| Last Author | Winkelmann J |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
Q47870612https://www.wikidata.org/wiki/Q47870612
Wikidata ID
