Biallelic loss-of-function OBSCN variants predispose individuals to severe, recurrent rhabdomyolysis
| dc.contributor.author | Aydin, Halil | |
| dc.contributor.pubmedID | 34957489 | en_US |
| dc.date.accessioned | 2022-08-11T10:44:37Z | |
| dc.date.available | 2022-08-11T10:44:37Z | |
| dc.date.issued | 2021 | |
| dc.identifier.issn | 0960-8966 | en_US |
| dc.identifier.issue | Supplement 1 | en_US |
| dc.identifier.uri | https://www.biorxiv.org/content/10.1101/2021.06.04.447044v1.full.pdf | |
| dc.identifier.uri | http://hdl.handle.net/11727/7310 | |
| dc.identifier.volume | 31 | en_US |
| dc.identifier.wos | 000697873700381 | en_US |
| dc.language.iso | eng | en_US |
| dc.relation.journal | NEUROMUSCULAR DISORDERS | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | Biallelic loss-of-function OBSCN variants predispose individuals to severe, recurrent rhabdomyolysis | en_US |
| dc.type | conferenceObject | en_US |