Observational studyJournal of molecular neuroscience : MN2017

A Novel CCM1/KRIT1 Heterozygous Nonsense Mutation (c.1864C>T) Associated with Familial Cerebral Cavernous Malformation: a Genetic Insight from an 8-Year Continuous Observational Study.

Chenlong Yang et al.PubMed ↗Publisher ↗

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