Assessment of Bone Mineral Status in Children With Marfan Syndrome

Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder with skeletal involvement. It is caused by mutations in fibrillin1 (FBN1) gene resulting in activation of TGF-β, which developmentally regulates bone mass and matrix properties. There is no consensus regarding bone mineralizat...

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Bibliografski detalji
Glavni autori: Grover, Monica, Brunetti-Pierri, Nicola, Belmont, John, Phan, Kelly, Tran, Alyssa, Shypailo, Roman J, Ellis, Kenneth J, Lee, Brendan H
Format: Artigo
Jezik:Inglês
Izdano: Wiley Subscription Services, Inc., A Wiley Company 2012
Teme:
Research Articles
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3429634/
https://ncbi.nlm.nih.gov/pubmed/22887731
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.35540
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