Dietary phosphate supplement does not rescue skeletal phenotype in a mouse model for craniometaphyseal dysplasia

BACKGROUND: Mutations in the human progressive ankylosis gene (ANKH; Mus musculus ortholog Ank) have been identified as cause for craniometaphyseal dysplasia (CMD), characterized by progressive thickening of craniofacial bones and flared metaphyses of long bones. We previously reported a knock-in (K...

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Detalles Bibliográficos
Autores principales: Liu, Yaling, Dutra, Eliane H., Reichenberger, Ernst J., Chen, I-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080755/
https://www.ncbi.nlm.nih.gov/pubmed/27784318
http://dx.doi.org/10.1186/s12952-016-0061-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080755/
https://www.ncbi.nlm.nih.gov/pubmed/27784318
http://dx.doi.org/10.1186/s12952-016-0061-0

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