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Mehmet Saim Kazan

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Case report Open access Sep 2026

Pediatric Familial Cerebral Cavernous Malformation Associated With a Novel KRIT1 Initiation‐Region Frameshift Variant

Familial cerebral cavernous malformation is an autosomal dominant vascular disorder with age‐dependent penetrance and marked intrafamilial variability and genotype–phenotype correlations remain limited.

Özlem Yayıcı Köken, M. S. Yanartaş, H. Aygün et al. · 0 citations

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