| Property | Value |
|---|
| Working Groups |  Winkelmann |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  27839873 |
| DOI |  10.1016/j.ajhg.2016.10.010 |
| Publication Year | 2016 |
| Title | Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia.  |
| Journal | American journal of human genetics |
| ISSN | 0002-9297 |
| ESSN | 1537-6605 |
| URL | https://www.ncbi.nlm.nih.gov/pubmed/?term=27839873%5Buid%5D |
| Pages | 1377-1387 |
| Issue | 6 |
| Volume | 99 |
| Journal Abbreviation | Am J Hum Genet |
| Authors | Zech M, Boesch S, Maier EM, Borggraefe I, Vill K, Laccone F, Pilshofer V, Ceballos-Baumann A, Alhaddad B, Berutti R, Poewe W, Haack TB, Haslinger B, Strom TM, Winkelmann J |
| First Author | Zech M |
| Last Author | Winkelmann J |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
Q37480675https://www.wikidata.org/wiki/Q37480675
Wikidata ID
