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Clinical and animal research findings in pycnodysostosis and gene mutations of cathepsin K from 1996 to 2011
Cathepsin K (CTSK) is a member of the papain-like cysteine protease family. Mutations in the CTSK gene cause a rare autosomal recessive bone disorder called pycnodysostosis (OMIM 265800). In order to follow the advances in the research about CTSK and pycnodysostosis, we performed a literature retros...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113317/ https://www.ncbi.nlm.nih.gov/pubmed/21569238 http://dx.doi.org/10.1186/1750-1172-6-20 |