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Phenotypic Characterization of Murine Models of Cerebral Cavernous Malformations
Cerebral cavernous malformations (CCMs) are clusters of dilated capillaries that affect around 0.5% of the population. CCMs exist in two forms, sporadic and familial. Mutations in 3 documented genes, KRIT1 (CCM1), CCM2 and PDCD10 (CCM3), cause the autosomal dominant form of the disease, and somatic...
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| I publikationen: | Lab Invest |
|---|---|
| Huvudupphovsmän: | , , , , , , , , , , , , , , , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2018
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6309944/ https://ncbi.nlm.nih.gov/pubmed/29946133 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41374-018-0030-y |
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