The Prevalence of Malformations of Cortical Development in a Pediatric Hereditary Hemorrhagic Telangiectasia Population
Author:
Publisher
American Society of Neuroradiology (ASNR)
Subject
Clinical Neurology,Radiology Nuclear Medicine and imaging
Reference23 articles.
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2. The UK prevalence of hereditary haemorrhagic telangiectasia and its association with sex, socioeconomic status and region of residence: a population-based study
3. Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
4. Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
5. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 ( SMAD4)
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