A carregar...
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...
Na minha lista:
| Publicado no: | Am J Med Genet A |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
|
| Assuntos: | |
| Acesso em linha: | 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|