peripheral myelin protein 22 (PMP22) genotyping
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Contents
1
Clinical significance
2
More general terms
3
Additional terms
4
References
Clinical significance
Charcot-Marie-Tooth disease
,
hereditary neuropathy
with liability to pressure
palsies
More general terms
genotyping (allele testing)
Additional terms
peripheral myelin protein 22; PMP-22; growth arrest-specific protein 3; GAS-3 (PMP22, GAS3)
References
↑
Loinc :accession 35324-3
↑
Loinc :accession 35325-0
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