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A distinct subset of Atypical Spitz Tumors is characterized by BRAF mutation and loss of BAP1 expression
We recently reported that germline mutations in BAP1 cause a familial tumor syndrome characterized by high penetrance for melanocytic tumors with distinct clinical and histologic features. Melanocytic neoplasms in affected individuals harbored BRAF mutations, showed loss of BAP1 expression, and hist...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3354018/ https://ncbi.nlm.nih.gov/pubmed/22367297 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/PAS.0b013e3182498be5 |
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