Publication | Closed Access
Association of a polymorphism of the ACVRL1 gene with sporadic arteriovenous malformations of the central nervous system
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Citations
27
References
2006
Year
The results of this study link ACVRL1 (HHT Type 2 gene) to the formation of the clinically sporadic variants of vascular malformations of the CNS most commonly seen in patients with HHT, that is, AVMs and DAVFs.
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