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Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas

✍ Scribed by Tournier-Lasserve, Elisabeth; Couteulx, Sophie Laberge-le; Jung, Hans H.; Labauge, Pierre; Houtteville, Jean-Pierre; Lescoat, Christelle; Cecillon, Michaelle; Marechal, Emmanuelle; Joutel, Anne; Bach, Jean-François

Book ID
109515469
Publisher
Nature Publishing Group
Year
1999
Tongue
English
Weight
714 KB
Volume
23
Category
Article
ISSN
1061-4036

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## Abstract Cavernous vascular malformations may affect brain and out‐of‐brain tissues. In most cases, cerebral cavernous malformations (CCMs) involve the brain alone, and are rarely associated with skin hemangiomas, spinal cord, retinal, hepatic or vertebral lesions. CCMs can cause seizures, intra