| Property | Value |
|---|
| Working Groups |  Meitinger |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  28612835 |
| DOI |  10.1038/ejhg.2017.96 |
| Publication Year | 2017 |
| Title | Coexisting variants in OSTM1 and MANEAL cause a complex neurodegenerative disorder with NBIA-like brain abnormalities.  |
| Journal | European journal of human genetics : EJHG |
| ISSN | 1018-4813 |
| ESSN | 1476-5438 |
| URL | https://www.ncbi.nlm.nih.gov/pubmed/?term=28612835%5Buid%5D |
| Pages | 1092-1095 |
| Issue | 9 |
| Volume | 25 |
| Journal Abbreviation | Eur J Hum Genet |
| Authors | Herebian D, Alhaddad B, Seibt A, Schwarzmayr T, Danhauser K, Klee D, Harmsen S, Meitinger T, Strom TM, Schulz A, Mayatepek E, Haack TB, Distelmaier F |
| First Author | Herebian D |
| Last Author | Distelmaier F |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
Q50945534https://www.wikidata.org/wiki/Q50945534
Wikidata ID
