Novel KRIT1/CCM1 and MGC4607/CCM2 Gene Variants in Chinese Families With Cerebral Cavernous Malformations

Familial cerebral cavernous malformations (CCMs) are autosomal dominant disorders characterized by hemorrhagic strokes, recurrent headache, epilepsy, and focal neurological deficits. Genetic variants in KRIT1/CCM1, MGC4607/CCM2, and PDCD10/CCM3 genes contribute to CCMs. The clinical information of t...

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Detalles Bibliográficos
Autores principales: Wang, Kang, Wu, Dengchang, Zhang, Baorong, Zhao, Guohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308150/
https://www.ncbi.nlm.nih.gov/pubmed/30622508
http://dx.doi.org/10.3389/fneur.2018.01128

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308150/
https://www.ncbi.nlm.nih.gov/pubmed/30622508
http://dx.doi.org/10.3389/fneur.2018.01128

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