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  • Molecular assay reagents intended to identify deletions or duplications of the FIG4 phosphoinositide 5-phosphatase (FIG4) gene, located at chromosome 6q21, which encodes the protein polyphosphoinositide phosphatase. Genetic variants at this locus have been associated with amyotrophic lateral sclerosis type 11, polymicrogyria, bilateral occipital, Charcot-Marie-Tooth disease, type 4j, and yunis varon syndrome.
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