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peripheral myelin protein 22 (PMP22) gene mutation

Clinical significance: - Charcot-Marie-Tooth disease, hereditary neuropathy with liability to pressure palsies

Related

peripheral myelin protein 22 (PMP22) genotyping peripheral myelin protein 22; PMP-22; growth arrest-specific protein 3; GAS-3 (PMP22, GAS3)

General

gene mutation testing; gene mutation analysis

References

  1. CPT :accession 813224
  2. CPT :accession 813225
  3. CPT :accession 813226
  4. Loinc :accession 21727-3
  5. Loinc :accession 71728-1