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...

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Detalles Bibliográficos
Autores principales: Xue, Yang, Cai, Tao, Shi, Songtao, Wang, Weiguang, Zhang, Yanli, Mao, Tianqiu, Duan, Xiaohong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Review
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

Internet

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

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