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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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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2015
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| Témata: | |
| On-line přístup: | 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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