Novel Brain Arteriovenous Malformation Mouse Models for Type 1 Hereditary Hemorrhagic Telangiectasia
Novel Brain Arteriovenous Malformation Mouse Models for Type 1 Hereditary Hemorrhagic Telangiectasia
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United States: Public Library of Science
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Language
English
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United States: Public Library of Science
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Contents
Endoglin (ENG) is a causative gene of type 1 hereditary hemorrhagic telangiectasia (HHT1). HHT1 patients have a higher prevalence of brain arteriovenous malformation (AVM) than the general population and patients with other HHT subtypes. The pathogenesis of brain AVM in HHT1 patients is currently unknown and no specific medical therapy is available...
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Full title
Novel Brain Arteriovenous Malformation Mouse Models for Type 1 Hereditary Hemorrhagic Telangiectasia
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TN_cdi_plos_journals_1497948122
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1497948122
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ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0088511
