| Property | Value |
|---|
| Working Groups |  Meitinger |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  30401461 |
| DOI |  10.1016/j.ajhg.2018.10.005 |
| Publication Year | 2018 |
| Title | Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy.  |
| Journal | American journal of human genetics |
| ISSN | 0002-9297 |
| ESSN | 1537-6605 |
| URL | https://www.ncbi.nlm.nih.gov/pubmed/?term=30401461%5Buid%5D |
| Pages | 817-825 |
| Issue | 5 |
| Volume | 103 |
| Journal Abbreviation | Am J Hum Genet |
| Authors | Danhauser K, Alhaddad B, Makowski C, Piekutowska-Abramczuk D, Syrbe S, Gomez-Ospina N, Manning MA, Kostera-Pruszczyk A, Krahn-Peper C, Berutti R, Kovács-Nagy R, Gusic M, Graf E, Laugwitz L, Röblitz M, Wroblewski A, Hartmann H, Das AM, Bültmann E, Fang F, Xu M, Schatz UA, Karall D, Zellner H, Haberlandt E, Feichtinger RG, Mayr JA, Meitinger T, Prokisch H, Strom TM, Płoski R, Hoffmann GF, Pronicki M, Bonnen PE, Morlot S, Haack TB |
| First Author | Danhauser K |
| Last Author | Haack TB |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
Q58618777https://www.wikidata.org/wiki/Q58618777
Wikidata ID
