X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype
| Main Authors: | , , , , , , , , , , |
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| Format: | Journal article |
| Published: |
1999
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| _version_ | 1797070998944612352 |
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| author | Whyte, M Christie, P Podgornik, M Dixon, P Eddy, M Wooding, C Trump, D Grieff, M Mumm, S Shlessinger, D Thakker, R |
| author_facet | Whyte, M Christie, P Podgornik, M Dixon, P Eddy, M Wooding, C Trump, D Grieff, M Mumm, S Shlessinger, D Thakker, R |
| author_sort | Whyte, M |
| collection | OXFORD |
| description | |
| first_indexed | 2024-03-06T22:46:56Z |
| format | Journal article |
| id | oxford-uuid:5d8081b7-30cc-49f8-9317-45e5153df86c |
| institution | University of Oxford |
| last_indexed | 2024-03-06T22:46:56Z |
| publishDate | 1999 |
| record_format | dspace |
| spelling | oxford-uuid:5d8081b7-30cc-49f8-9317-45e5153df86c2022-03-26T17:34:50ZX-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotypeJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:5d8081b7-30cc-49f8-9317-45e5153df86cSymplectic Elements at Oxford1999Whyte, MChristie, PPodgornik, MDixon, PEddy, MWooding, CTrump, DGrieff, MMumm, SShlessinger, DThakker, R |
| spellingShingle | Whyte, M Christie, P Podgornik, M Dixon, P Eddy, M Wooding, C Trump, D Grieff, M Mumm, S Shlessinger, D Thakker, R X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype |
| title | X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype |
| title_full | X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype |
| title_fullStr | X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype |
| title_full_unstemmed | X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype |
| title_short | X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype |
| title_sort | x linked hypophosphatemia xlh mutations compromising phex structure reflect a severe phenotype |
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