| Property | Value |
|---|
| Working Groups |  Meitinger, Müller-Myhsok, Winkelmann |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  24995868 |
| DOI |  10.1016/j.ajhg.2014.06.005 |
| Publication Year | 2014 |
| Title | Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome.  |
| Journal | American journal of human genetics |
| ISSN | 0002-9297 |
| ESSN | 1537-6605 |
| URL | https://www.ncbi.nlm.nih.gov/pubmed/?term=24995868%5Buid%5D |
| Pages | 85-95 |
| Issue | 1 |
| Volume | 95 |
| Journal Abbreviation | Am J Hum Genet |
| Authors | Schulte EC, Kousi M, Tan PL, Tilch E, Knauf F, Lichtner P, Trenkwalder C, Högl B, Frauscher B, Berger K, Fietze I, Hornyak M, Oertel WH, Bachmann CG, Zimprich A, Peters A, Gieger C, Meitinger T, Müller-Myhsok B, Katsanis N, Winkelmann J |
| First Author | Schulte EC |
| Last Author | Winkelmann J |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
Q33858791https://www.wikidata.org/wiki/Q33858791
Wikidata ID
