Mice deleted for cell division cycle 73 gene develop parathyroid and uterine tumours: model for the hyperparathyroidism-jaw tumour syndrome

The hyperparathyroidism-jaw tumour (HPT-JT) syndrome is an autosomal dominant disorder characterized by occurrence of parathyroid tumours, often atypical adenomas and carcinomas, ossifying jaw fibromas, renal tumours and uterine benign and malignant neoplasms. HPT-JT is caused by mutations of the ce...

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Detalles Bibliográficos
Autores principales: Walls, G V, Stevenson, M, Lines, K E, Newey, P J, Reed, A A C, Bowl, M R, Jeyabalan, J, Harding, B, Bradley, K J, Manek, S, Chen, J, Wang, P, Williams, B O, Teh, B T, Thakker, R V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472200/
https://www.ncbi.nlm.nih.gov/pubmed/28288139
http://dx.doi.org/10.1038/onc.2017.43

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472200/
https://www.ncbi.nlm.nih.gov/pubmed/28288139
http://dx.doi.org/10.1038/onc.2017.43

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