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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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Bibliografiske detaljer
Udgivet i:Am J Med Genet A
Main Authors: Manole, Athanasios K., Forrester, Vernon J., Zlotoff, Barrett J., Hart, Blaine L., Morrison, Leslie A.
Format: Artigo
Sprog:Inglês
Udgivet: 2020
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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