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bn:04726731n
Noun Concept
JA
No term available
EN
Syndrome that is characterized by progressive proximal muscle weakness, steolytic bone lesions consistent with Paget disease, and frontotemporal dementia and has physical basis in mutation in the valosin containing protein (VCP) Wikidata
Relations
Sources
IS A
希少疾患
症候群
GNEミオパチー
前頭側頭型認知症
GENETIC ASSOCIATION
EN
hnRNPA1
EN
HNRPA2B1
EN
Valosin-containing protein
HEALTH SPECIALTY
神経学

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