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Molecular assay reagents intended to identify gene variants associated with lissencephalies, a collection of cortical malformations involving abnormal neuronal cell migration and resulting in the loss of the convolutions of the cerebral cortex. Genetic variants at multiple loci have been associated with lissencephalies. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple lissencephaly-associated loci simultaneously.
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