| Property | Value |
|---|
| Working Groups |  Winkelmann |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  31636353 |
| DOI |  10.1038/s41467-019-12620-9 |
| Publication Year | 2019 |
| Title | Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.  |
| Journal | Nature communications |
| ESSN | 2041-1723 |
| URL | https://www.ncbi.nlm.nih.gov/pubmed/?term=31636353%5Buid%5D |
| Pages | 4790 |
| Issue | 1 |
| Volume | 10 |
| Journal Abbreviation | Nat Commun |
| Authors | Wagner M, Osborn DPS, Gehweiler I, Nagel M, Ulmer U, Bakhtiari S, Amouri R, Boostani R, Hentati F, Hockley MM, Hölbling B, Schwarzmayr T, Karimiani EG, Kernstock C, Maroofian R, Müller-Felber W, Ozkan E, Padilla-Lopez S, Reich S, Reichbauer J, Darvish H, Shahmohammadibeni N, Tafakhori A, Vill K, Zuchner S, Kruer MC, Winkelmann J, Jamshidi Y, Schüle R |
| First Author | Wagner M |
| Last Author | Schüle R |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
Q90859270https://www.wikidata.org/wiki/Q90859270
Wikidata ID
