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A novel CCM3 mutation associated with cerebral cavernous malformation in a Chinese family
BACKGROUND: Cerebral cavernous malformation (CCM), especially the familial form, is a relatively rare congenital and occult vascular disease of the central nervous system. The familial form of CCM has been linked to three different genes: KRIT1/CCM1, MGC4607/CCM2, and PDCD10/CCM3; however, the genet...
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| Pubblicato in: | Ther Adv Neurol Disord |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
SAGE Publications
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6997961/ https://ncbi.nlm.nih.gov/pubmed/32071616 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1756286420902664 |
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