Juvenile Paget’s Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor Sp7)

Juvenile Paget’s disease (JPD) became in 1974 the commonly used name for ultra-rare heritable occurrences of rapid bone remodeling throughout of the skeleton that present in infancy or early childhood as fractures and deformity hallmarked biochemically by marked elevation of serum alkaline phosphata...

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Publicado en:Bone
Main Authors: Whyte, Michael P., Campeau, Philippe M., McAlister, William H., Roodman, G. David, Kurihara, Nori, Nenninger, Angela, Duan, Shenghui, Gottesman, Gary S., Bijanki, Vinieth N., Sedighi, Homer, Veis, Deborah J., Mumm, Steven
Formato: Artigo
Idioma:Inglês
Publicado: 2020
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8054448/
https://ncbi.nlm.nih.gov/pubmed/32298837
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2020.115364
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