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Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets.
A new dominant mutation in the laboratory mouse, hypophosphatemia (gene symbol Hyp), has been identified. The Hyp gene is located on the X-chromosome and maps at the distal end. Mutant mice are characterized by hypophosphatemia, bone changes resembling rickets, diminished bone ash, dwarfism, and hig...
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| Izdano u: | Proc Natl Acad Sci U S A |
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| Glavni autori: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
National Academy of Sciences
1976
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC431589/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/188049/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.73.12.4667 |
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