| Property | Value |
|---|
| Working Groups |  Dichgans, Meitinger |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  27545679 |
| DOI |  10.1016/j.ajhg.2016.06.026 |
| Publication Year | 2016 |
| Title | Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy.  |
| Journal | American journal of human genetics |
| ISSN | 0002-9297 |
| ESSN | 1537-6605 |
| URL | https://www.ncbi.nlm.nih.gov/pubmed/?term=27545679%5Buid%5D |
| Pages | 735-743 |
| Issue | 3 |
| Volume | 99 |
| Journal Abbreviation | Am J Hum Genet |
| Authors | Haack TB, Ignatius E, Calvo-Garrido J, Iuso A, Isohanni P, Maffezzini C, Lönnqvist T, Suomalainen A, Gorza M, Kremer LS, Graf E, Hartig M, Berutti R, Paucar M, Svenningsson P, Stranneheim H, Brandberg G, Wedell A, Kurian MA, Hayflick SA, Venco P, Tiranti V, Strom TM, Dichgans M, Horvath R, Holinski-Feder E, Freyer C, Meitinger T, Prokisch H, Senderek J, Wredenberg A, Carroll CJ, Klopstock T |
| First Author | Haack TB |
| Last Author | Klopstock T |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
Q37230703https://www.wikidata.org/wiki/Q37230703
Wikidata ID
