Cerebral Cavernous Malformations Develop Through Clonal Expansion of Mutant Endothelial Cells
Author:
Affiliation:
1. From the Molecular Genetics and Microbiology Department (M.R.D., D.A.S., D.A.M.), Duke University School of Medicine, Durham, NC.
2. Medical Scientist Training Program (M.R.D.), Duke University School of Medicine, Durham, NC.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine,Physiology
Reference31 articles.
1. Etiology and Genetics of Congenital Vascular Lesions
2. Vascular Anomalies
3. Mutations in the Gene Encoding KRIT1, a Krev-1/rap1a Binding Protein, Cause Cerebral Cavernous Malformations (CCM1)
4. Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas
5. Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous Malformations
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