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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Detalles Bibliográficos
Autores principales: Jiang, Xiao-yu, Zhang, Ying, Yin, Xiang, Nan, Di, Wang, Xu, Feng, Jia-chun, Miao, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997961/
https://www.ncbi.nlm.nih.gov/pubmed/32071616
http://dx.doi.org/10.1177/1756286420902664

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