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Q57484322-20096945-2AEA-45B8-8F4B-CF706F956F0A
Q57484322-20096945-2AEA-45B8-8F4B-CF706F956F0A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-20096945-2AEA-45B8-8F4B-CF706F956F0A
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P2860
Q57484322-20096945-2AEA-45B8-8F4B-CF706F956F0A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-20096945-2AEA-45B8-8F4B-CF706F956F0A
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wasDerivedFrom
cddc5db81dd1747d2d348fa8b14e619569132815
P2860
Neurofascin 140 is an embryonic neuronal neurofascin isoform that promotes the assembly of the node of Ranvier