| Property | Value |
|---|
| Working Groups |  Haass, Meitinger, Winkelmann |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  25604855 |
| DOI |  10.1038/ejhg.2014.300 |
| Publication Year | 2015 |
| Title | Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease.  |
| Journal | European journal of human genetics : EJHG |
| ISSN | 1018-4813 |
| ESSN | 1476-5438 |
| URL | https://www.ncbi.nlm.nih.gov/pubmed/?term=25604855%5Buid%5D |
| Pages | 1328-33 |
| Issue | 10 |
| Volume | 23 |
| Journal Abbreviation | Eur J Hum Genet |
| Authors | Schulte EC, Fukumori A, Mollenhauer B, Hor H, Arzberger T, Perneczky R, Kurz A, Diehl-Schmid J, Hüll M, Lichtner P, Eckstein G, Zimprich A, Haubenberger D, Pirker W, Brücke T, Bereznai B, Molnar MJ, Lorenzo-Betancor O, Pastor P, Peters A, Gieger C, Estivill X, Meitinger T, Kretzschmar HA, Trenkwalder C, Haass C, Winkelmann J |
| First Author | Schulte EC |
| Last Author | Winkelmann J |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
Q36116716https://www.wikidata.org/wiki/Q36116716
Wikidata ID
