Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: A causative mutation?
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference26 articles.
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2. Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2020-12
3. Two Novel CCM2 Heterozygous Mutations Associated with Cerebral Cavernous Malformation in a Chinese Family;Journal of Molecular Neuroscience;2019-01-30
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