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  • Molecular assay reagents intended to identify gene variants associated with familial cerebral cavernous malformations, vascular malformations in the central nervous system characterized by clusters of enlarged and abnormally structured capillaries. Genetic variants at multiple loci have been associated with cerebral cavernous malformations. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple cerebral cavernous malformation-associated loci simultaneously.
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