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Q57484322-0B30441A-B615-4179-BF32-000DB7D47F5E
Q57484322-0B30441A-B615-4179-BF32-000DB7D47F5E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-0B30441A-B615-4179-BF32-000DB7D47F5E
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P2860
Q57484322-0B30441A-B615-4179-BF32-000DB7D47F5E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-0B30441A-B615-4179-BF32-000DB7D47F5E
rank
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wasDerivedFrom
cddc5db81dd1747d2d348fa8b14e619569132815
P2860
Axon-glia interactions and the domain organization of myelinated axons requires neurexin IV/Caspr/Paranodin.