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-...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: 2004
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2859190/
https://ncbi.nlm.nih.gov/pubmed/15029877
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados