Renal dysfunction rodcone dystrophy and sensorineural hearing loss caused by a mutation in RRM2B
dc.citation.doi | 10.1002/HUMU.24094 | |
dc.citation.epage | 6 | |
dc.citation.spage | 1 | |
dc.contributor.author | Lisa Roberts | |
dc.contributor.author | Stephanie Julius | |
dc.contributor.author | Shrinav Dawlat | |
dc.contributor.author | Safiye Yildiz | |
dc.contributor.author | Jorge Da Rocha | |
dc.contributor.author | E et al | |
dc.date.accessioned | 2023-10-06T12:11:43Z | |
dc.date.available | 2023-10-06T12:11:43Z | |
dc.identifier.citation | WOS | |
dc.identifier.issn | 1059-7794 | |
dc.identifier.uri | https://hdl.handle.net/10539/36496 | |
dc.journal.title | HUMAN MUTATION | |
dc.journal.volume | - | |
dc.title | Renal dysfunction rodcone dystrophy and sensorineural hearing loss caused by a mutation in RRM2B |
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