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Immunohistochemical assessment of parafibromin in mouse and human tissues
Parafibromin is a protein encoded by the HRPT2 oncosuppressor gene, whose mutation causes the hyperparathyroidism–jaw tumour syndrome, characterized by the occurrence of parathyroid adenoma or carcinoma, fibro-osseous jaw tumours, and renal neoplastic and non-neoplastic abnormalities. Non-morphologi...
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| Principais autores: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2048996/ https://ncbi.nlm.nih.gov/pubmed/17118068 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-7580.2006.00657.x |
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