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Cutaneous findings of familial cerebral cavernous malformation syndrome due to the common Hispanic mutation
Familial cerebral cavernous malformations due to the common Hispanic mutation (FCCM1-CHM) is an endemic condition among the Hispanic population of the Southwestern United States associated with significant morbidity and mortality. Cutaneous vascular malformations (CVMs) can be found in individuals w...
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| Udgivet i: | Am J Med Genet A |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8208466/ https://ncbi.nlm.nih.gov/pubmed/32100472 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.61519 |
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