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Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization
In humans, SOX9 heterozygous mutations cause the severe skeletal dysmorphology syndrome campomelic dysplasia. Except for clinical descriptions, little is known about the pathogenesis of this disease. We have generated heterozygous Sox9 mutant mice that phenocopy most of the skeletal abnormalities of...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The National Academy of Sciences
2001
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC34415/ https://ncbi.nlm.nih.gov/pubmed/11371614 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.111092198 |
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