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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Pubblicato in:	Proc Natl Acad Sci U S A
Autori principali:	Eicher, E M, Southard, J L, Scriver, C R, Glorieux, F H
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	National Academy of Sciences 1976
Soggetti:	Research Article
Accesso online:	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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