Identification of a novel KRIT1 mutation in an Italian family with cerebral cavernous malformation by the protein truncation test
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
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2. De Novo MGC4607 Gene Heterozygous Missense Variants in a Child with Multiple Cerebral Cavernous Malformations;Journal of Molecular Neuroscience;2012-03-14
3. Surgical Management of Cavernous Malformations of the Nervous System;Schmidek and Sweet Operative Neurosurgical Techniques;2012
4. Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation;Brain Pathology;2010-10-04
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