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bn:06255390n
Noun Concept
IT
No term available
EN
Charcot-Marie-Tooth disease type 1 that has material basis in duplication of, or mutation in, the gene encoding peripheral myelin protein-22 (PMP22) Wikidata
Relations
Sources
IS A
malattia genetica
EN
Charcot-Marie-Tooth disease type 1
HEALTH SPECIALTY
neurologia

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