New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice

X-linked hypophosphatemic rickets (XLH) in humans is caused by mutations in the PHEX gene. Previously, three mutations in the mouse Phex gene have been reported: Phex(Hyp), Gy, and Phex(Ska1). Here we report analysis of two new spontaneous mutations in the mouse Phex gene, Phex(Hyp-2J) and Phex(Hyp-...

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Autori principali: Lorenz-Depiereux, Bettina, Guido, Victoria E., Johnson, Kenneth R., Zheng, Qing Yin, Gagnon, Leona H., Bauschatz, Joiel D., Davisson, Muriel T., Washburn, Linda L., Donahue, Leah Rae, Strom, Tim M., Eicher, Eva M.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2004
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2859190/
https://ncbi.nlm.nih.gov/pubmed/15029877
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