| Property | Value |
|---|
| Working Groups |  Meitinger |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  25658047 |
| DOI |  10.1016/j.ajhg.2014.12.023 |
| Publication Year | 2015 |
| Title | COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiency.  |
| Journal | American journal of human genetics |
| ISSN | 0002-9297 |
| ESSN | 1537-6605 |
| URL | https://www.ncbi.nlm.nih.gov/pubmed/?term=25658047%5Buid%5D |
| Pages | 309-17 |
| Issue | 2 |
| Volume | 96 |
| Journal Abbreviation | Am J Hum Genet |
| Authors | Brea-Calvo G, Haack TB, Karall D, Ohtake A, Invernizzi F, Carrozzo R, Kremer L, Dusi S, Fauth C, Scholl-Bürgi S, Graf E, Ahting U, Resta N, Laforgia N, Verrigni D, Okazaki Y, Kohda M, Martinelli D, Freisinger P, Strom TM, Meitinger T, Lamperti C, Lacson A, Navas P, Mayr JA, Bertini E, Murayama K, Zeviani M, Prokisch H, Ghezzi D |
| First Author | Brea-Calvo G |
| Last Author | Ghezzi D |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
Q35059346https://www.wikidata.org/wiki/Q35059346
Wikidata ID
