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Neonatal High Bone Mass With First Mutation Of The NF-κB Complex: Heterozygous De Novo Missense (p.Asp512Ser) RELA (Rela/p65)

Heritable disorders that feature high bone mass (HBM) are rare. The etiology is typically a mutation(s) within a gene that regulates the differentiation and function of osteoblasts (OBs) or osteoclasts (OCs). Nevertheless, the molecular basis is unknown for approximately one-fifth of such entities....

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Detaylı Bibliyografya
Yayımlandı:	J Bone Miner Res
Asıl Yazarlar:	Frederiksen, Anja L., Larsen, Martin J., Brusgaard, Klaus, Novack, Deborah V., Knudsen, Peter Juel Thiis, Schrøder, Henrik Daa, Qiu, Weimin, Eckhardt, Christina, McAlister, William H., Kassem, Moustapha, Mumm, Steven, Frost, Morten, Whyte, Michael P.
Materyal Türü:	Artigo
Dil:	Inglês
Baskı/Yayın Bilgisi:	2015
Konular:	Article
Online Erişim:	https://ncbi.nlm.nih.gov/pmc/articles/PMC5310715/ https://ncbi.nlm.nih.gov/pubmed/26178921 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.2590
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Neonatal High Bone Mass With First Mutation Of The NF-κB Complex: Heterozygous De Novo Missense (p.Asp512Ser) RELA (Rela/p65)

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