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Q57484322-167193E6-B31D-472E-8A57-FA23C445B849
Q57484322-167193E6-B31D-472E-8A57-FA23C445B849
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-167193E6-B31D-472E-8A57-FA23C445B849
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P1433
Q57484322-167193E6-B31D-472E-8A57-FA23C445B849
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-167193E6-B31D-472E-8A57-FA23C445B849
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
4c30540ed9f848fc2c2839f1cee643c7476f1750
P1433
Human Molecular Genetics