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Spectrum of SMARCB1/INI1 Mutations in Familial and Sporadic Rhabdoid Tumors
BACKGROUND: Germline mutations and deletions of SMARCB1/INI1 in chromosome band 22q11.2 predispose patients to rhabdoid tumor and schwannomatosis. Previous estimates suggested that 15–20% of rhabdoid tumors were caused by an underlying germline abnormality of SMARCB1. However, these studies were lim...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3086793/ https://ncbi.nlm.nih.gov/pubmed/21108436 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pbc.22831 |
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