Cover, Volume 43, Issue 2

dc.contributor.authorSarafrazi, Soodabeh
dc.contributor.authorDaugherty, Sean C.
dc.contributor.authorMiller, Nicole
dc.contributor.authorBoada, Patrick
dc.contributor.authorCarpenter, Thomas O.
dc.contributor.authorChunn, Lauren
dc.contributor.authorDill, Kariena
dc.contributor.authorEcons, Michael J.
dc.contributor.authorEisenbeis, Scott
dc.contributor.authorImel, Erik A.
dc.contributor.authorJohnson, Britt
dc.contributor.authorKiel, Mark J.
dc.contributor.authorKrolczyk, Stan
dc.contributor.authorRamesan, Prameela
dc.contributor.authorTruty, Rebecca
dc.contributor.authorSabbagh, Yves
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2024-11-21T09:11:39Z
dc.date.available2024-11-21T09:11:39Z
dc.date.issued2022
dc.description.abstractThe 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.versionFinal published version
dc.identifier.citationSarafrazi 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.urihttps://hdl.handle.net/1805/44634
dc.language.isoen_US
dc.publisherWiley
dc.relation.isversionof10.1002/humu.24334
dc.relation.journalHuman Mutation
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourcePublisher
dc.subjectPHEX gene
dc.subjectX-linked hypophosphatemia
dc.titleCover, Volume 43, Issue 2
dc.typeArticle
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