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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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Bibliografische gegevens
Gepubliceerd in:Front Neurol
Hoofdauteurs: Wang, Kang, Wu, Dengchang, Zhang, Baorong, Zhao, Guohua
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Frontiers Media S.A. 2018
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6308150/
https://ncbi.nlm.nih.gov/pubmed/30622508
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2018.01128
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