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peripheral myelin protein 22 (PMP22) genotyping
Clinical significance: - Charcot-Marie-Tooth disease, hereditary neuropathy with liability to pressure palsiesRelated
peripheral myelin protein 22; PMP-22; growth arrest-specific protein 3; GAS-3 (PMP22, GAS3)General
genotyping (allele testing)References
- Loinc :accession 35324-3
- Loinc :accession 35325-0