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Q57484322-BB39821E-FFE8-4EAC-9377-2C877767FAF4
Q57484322-BB39821E-FFE8-4EAC-9377-2C877767FAF4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-BB39821E-FFE8-4EAC-9377-2C877767FAF4
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P921
Q57484322-BB39821E-FFE8-4EAC-9377-2C877767FAF4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-BB39821E-FFE8-4EAC-9377-2C877767FAF4
rank
NormalRank
type
BestRank
Statement
P921
molecular biology