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  • Molecular assay reagents intended to identify gene variants associated with Rett syndrome and Angelman syndrome, two neurologic disorders with substantial phenotypic overlap including developmental delay, seizures, and autistic behaviors. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Rett syndrome-associated and Angelman syndrome loci simultaneously for the purpose of distinguishing between these diseases.
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