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  • Molecular assay reagents intended to identify mutations in the Usher syndrome 2A (USH2A) gene, located at chromosome 1q41, which encodes for a protein that is an important component of basement membranes and whose function is not well established. This inherited genetic mutation has been identified in patients with Usher\'s syndrome type 2; it is also associated with nonsyndromic retinitis pigmentosa (type 15).
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