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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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| Vydáno v: | Neuroradiol J |
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| Hlavní autoři: | , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
SAGE Publications
2015
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| Témata: | |
| On-line přístup: | 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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