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Molecular assay reagents intended to identify deletions or duplications of the anoctamin 5 (ANO5) gene, located at chromosome 11p14.3, which encodes the protein anoctamin-5. Genetic variants at this locus have been associated with Miyoshi muscular dystrophy 3, limb-girdle muscular dystrophy, type 2L, and osteogenesis imperfecta levin type.
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