Cover, Volume 43, Issue 2
dc.contributor.author | Sarafrazi, Soodabeh | |
dc.contributor.author | Daugherty, Sean C. | |
dc.contributor.author | Miller, Nicole | |
dc.contributor.author | Boada, Patrick | |
dc.contributor.author | Carpenter, Thomas O. | |
dc.contributor.author | Chunn, Lauren | |
dc.contributor.author | Dill, Kariena | |
dc.contributor.author | Econs, Michael J. | |
dc.contributor.author | Eisenbeis, Scott | |
dc.contributor.author | Imel, Erik A. | |
dc.contributor.author | Johnson, Britt | |
dc.contributor.author | Kiel, Mark J. | |
dc.contributor.author | Krolczyk, Stan | |
dc.contributor.author | Ramesan, Prameela | |
dc.contributor.author | Truty, Rebecca | |
dc.contributor.author | Sabbagh, Yves | |
dc.contributor.department | Medicine, School of Medicine | |
dc.date.accessioned | 2024-11-21T09:11:39Z | |
dc.date.available | 2024-11-21T09:11:39Z | |
dc.date.issued | 2022 | |
dc.description.abstract | The cover image is based on the Research Article Novel PHEX gene locus-specific database: Comprehensive characterization of vast number of variants associated with X-linked hypophosphatemia (XLH) by Yves Sabbagh et al., https://doi.org/10.1002/humu.24296. | |
dc.eprint.version | Final published version | |
dc.identifier.citation | Sarafrazi S, Daugherty SC, Miller N, et al. Cover, Volume 43, Issue 2. Human Mutation. 2022;43(2):i-i. doi:10.1002/humu.24334 | |
dc.identifier.uri | https://hdl.handle.net/1805/44634 | |
dc.language.iso | en_US | |
dc.publisher | Wiley | |
dc.relation.isversionof | 10.1002/humu.24334 | |
dc.relation.journal | Human Mutation | |
dc.rights | Attribution 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Publisher | |
dc.subject | PHEX gene | |
dc.subject | X-linked hypophosphatemia | |
dc.title | Cover, Volume 43, Issue 2 | |
dc.type | Article |