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Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene
Multiple familial meningiomas occur in rare genetic syndromes, particularly neurofibromatosis type 2. The association of meningiomas and cerebral cavernous malformations (CCMs) has been reported in few patients in the medical literature. The purpose of our study is to corroborate a preferential asso...
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| 出版年: | Neuroradiol J |
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| 主要な著者: | , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
SAGE Publications
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4757286/ https://ncbi.nlm.nih.gov/pubmed/26246098 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1971400915591688 |
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