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A Chinese Family With Cerebral Cavernous Malformation Caused by a Frameshift Mutation of the CCM1 Gene: A Case Report and Review of the Literature

BACKGROUND: Familial cerebral cavernous malformation (FCCM) is a vascular malformation disease closely linked to three identified genes: KRIT1/CCM1, MGC4607/CCM2 and PDCD10/CCM3. Over the past decade, a few cases of cerebral cavernous malformation (CCM) caused by different gene mutations have been r...

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Detalles Bibliográficos
Autores principales:	Liu, Wenyu, Liu, Ming, Lu, Di, Wang, Jiwei, Cao, Zexin, Liu, Xuchen, Feng, Zichao, Huang, Bin, Wang, Xinyu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Neurology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013744/ https://www.ncbi.nlm.nih.gov/pubmed/35444609 http://dx.doi.org/10.3389/fneur.2022.795514

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