Polymorphisms in ACVRL1 and Endoglin Genes are Not Associated with Sporadic and HHT-Related Brain AVMs in Dutch Patients

We aimed to replicate the association of the IVS3-35A>G polymorphism in the activin receptor-like kinase (ACVRL) 1 gene and the 207G>A polymorphism in the endoglin (ENG) gene with sporadic brain arteriovenous malformations (BAVM) in Dutch BAVM patients. In addition, we assessed whether these polymorphisms contribute to the risk of BAVM in patients with hereditary haemorrhagic telangiectasia type 1 (HHT1). We genotyped 143 Dutch sporadic BAVM patients and 360 healthy volunteers for four variants in the ACVRL1 gene including IVS3-35A>G and two variants in the ENG gene including 207G>... Mehr ...

Verfasser: Boshuisen, Kim
Brundel, Manon
de Kovel, Carolien GF
Letteboer, Tom G
Rinkel, Gabriel JE
Westermann, Cornelis JJ
Kim, Helen
Pawlikowska, Ludmila
Koeleman, Bobby PC
Klijn, Catharina JM
Dokumenttyp: Artikel
Erscheinungsdatum: 2013
Reihe/Periodikum: Translational Stroke Research, vol 4, iss 3
Verlag/Hrsg.: eScholarship
University of California
Schlagwörter: Pharmacology and Pharmaceutical Sciences / Biomedical and Clinical Sciences / Genetics / Pediatric / Neurosciences / 2.1 Biological and endogenous factors / Aetiology / Activin Receptors / Type II / Antigens / CD / Case-Control Studies / Endoglin / Female / Genotype / Humans / Intracranial Arteriovenous Malformations / Male / Middle Aged / Netherlands / Pedigree / Polymorphism / Single Nucleotide / Receptors / Cell Surface / Telangiectasia / Hereditary Hemorrhagic / Arteriovenous malformations / Neurogenetics / Cerebrovascular disease / Clinical Sciences / Public Health and Health Services
Sprache: unknown
Permalink: https://search.fid-benelux.de/Record/base-27570947
Datenquelle: BASE; Originalkatalog
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Link(s) : https://escholarship.org/uc/item/76g2f81d