Crystal structure of the N-terminal domain of human CDC73 and its implications for the hyperparathyroidism-jaw tumor (HPT-JT) syndrome
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Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-15715-9.pdf
Reference43 articles.
1. Carpten, J. D. et al. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nature genetics 32, 676–680, https://doi.org/10.1038/ng1048 (2002).
2. Newey, P. J., Bowl, M. R. & Thakker, R. V. Parafibromin - functional insights. Journal of Internal Medicine 266, 84–98, https://doi.org/10.1111/j.1365-2796.2009.02107.x (2009).
3. Newey, P. J., Bowl, M. R., Cranston, T. & Thakker, R. V. Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors. Human mutation 31, 295–307, https://doi.org/10.1002/humu.21188 (2010).
4. Chen, Y. et al. CDC73 gene mutations in sporadic ossifying fibroma of the jaws. Diagnostic pathology 11, 91, https://doi.org/10.1186/s13000-016-0532-0 (2016).
5. Gill, A. J. Understanding the genetic basis of parathyroid carcinoma. Endocrine pathology 25, 30–34, https://doi.org/10.1007/s12022-013-9294-3 (2014).
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