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  • Molecular assay reagents intended to identify mutations in Charcot-Marie-Tooth neuropathy 1B (CMT1B) gene (also known as the myelin protein zero gene [MPZ]), located at chromosome 1q22, which encodes for myelin protein zero, a major structural protein of peripheral myelin. Mutations at this locus have been identified in patients with various forms of hereditary mutant sensory neuropathy (HMSN1-3), such as Charcot-Marie-Tooth disease.
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