טוען...
SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis
BACKGROUND: Schwannomatosis is a disease characterized by multiple non-vestibular schwannomas. Although biallelic NF2 mutations are found in schwannomas, no germ line event is detected in schwannomatosis patients. In contrast, germline mutations of the SMARCB1 (INI1) tumor suppressor gene were descr...
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| Main Authors: | , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2011
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3037869/ https://ncbi.nlm.nih.gov/pubmed/21255467 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-11-9 |
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