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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...

詳細記述

保存先:
書誌詳細
出版年:Bone
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: 2020
主題:
オンライン・アクセス: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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