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bn:06256252n
Noun Concept
IT
No term available
EN
Charcot-Marie-Tooth disease type 1 that has material basis in heterozygous mutation in the gene encoding myelin protein zero (MPZ) Wikidata
Relations
Sources
IS A
malattia rara
EN
Charcot-Marie-Tooth disease type 1
GENETIC ASSOCIATION
MPZ
HEALTH SPECIALTY
neurologia

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