peripheral myelin protein 22 (PMP22) gene mutation

Clinical significance

• Charcot-Marie-Tooth disease, hereditary neuropathy with liability to pressure palsies

More general terms

• gene mutation testing; gene mutation analysis

Additional terms

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