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  • Molecular assay reagents intended to identify mutations in the neurofibromin 2 (NF2) gene, located at chromosome 22q12.2, which encodes for the protein merlin (also known as schwannomin), made in Schwann cells. Merlin plays a role in controlling cell shape, cell movement, and communication between cells. Mutations at this locus have been identified in patients with neurofibromatosis type 2 (NF2), a young adult onset disease characterized by bilateral vestibular neoplasms of the Schwann cells of neurons (i.e., schwannomas) causing tinnitus, hearing loss, and loss of balance.
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