Multi-dimensional bone density phenotyping reveals new insights in to genetic regulation of the pediatric skeleton

Osteoporosis is a complex disease with developmental origins. It is therefore important to understand the genetic contribution to pediatric areal bone mineral density (aBMD). Individual skeletal site phenotyping has been primarily used to identify pediatric aBMD loci. However, this approach is limit...

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Pubblicato in:J Bone Miner Res
Autori principali: Mitchell, Jonathan A., Chesi, Alessandra, Cousminer, Diana L., McCormack, Shana E., Kalkwarf, Heidi J., Lappe, Joan M., Gilsanz, Vicente, Oberfield, Sharon E., Shepherd, John A., Kelly, Andrea, Zemel, Babette S., Grant, Struan F.A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2018
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7473448/
https://ncbi.nlm.nih.gov/pubmed/29240982
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.3362
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