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The genetic implication of scoliosis in osteogenesis imperfecta: a review

Osteogenesis imperfecta (OI) is a kind of heritable connective tissue disorder, including blue sclerae, hearing loss, skeletal dysplasia causing bone fragility and deformities. It is typically caused by collagen related gene mutations, which could lead to bone formation abnormalities. Scoliosis is o...

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Bibliografiske detaljer
Udgivet i:J Spine Surg
Main Authors: Liu, Gang, Chen, Jia, Zhou, Yangzhong, Zuo, Yuzhi, Liu, Sen, Chen, Weisheng, Wu, Zhihong, Wu, Nan
Format: Artigo
Sprog:Inglês
Udgivet: AME Publishing Company 2017
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5760423/
https://ncbi.nlm.nih.gov/pubmed/29354746
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/jss.2017.10.01
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