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Specific ablation of mouse Fam20C in cells expressing type I collagen leads to skeletal defects and hypophosphatemia

FAM20C mutations in humans cause Raine syndrome and our previous studies showed that global inactivation of mouse Fam20C led to bone and dental defects. By crossbreeding 2.3  kb Col 1a1-Cre mice with Fam20C (flox/flox) mice, we created 2.3  kb Col 1a1-Cre;Fam20C (foxl/flox) (cKO) mice, in which Fam2...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Liu, Peihong, Ma, Su, Zhang, Hua, Liu, Chao, Lu, Yongbo, Chen, Li, Qin, Chunlin
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5472603/
https://ncbi.nlm.nih.gov/pubmed/28620244
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-03960-x
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