Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter gene

Spondylolysis is a fracture in part of the vertebra with a reported prevalence of about 3–6% in the general population. Genetic etiology of this disorder remains unknown. The present study was aimed at identifying genomic mutations in patients with dysplastic spondylolysis as well as the potential p...

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Detaylı Bibliyografya
Yayımlandı:Proc Natl Acad Sci U S A
Asıl Yazarlar: Cai, Tao, Yang, Liu, Cai, Wanshi, Guo, Sen, Yu, Ping, Li, Jinchen, Hu, Xueyu, Yan, Ming, Shao, Qianzhi, Jin, Yan, Sun, Zhong Sheng, Luo, Zhuo-Jing
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2015
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4491795/
https://ncbi.nlm.nih.gov/pubmed/26077908
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1502454112
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