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Q57484322-3EDE9DB8-1CB7-41BE-8346-8835D165264A
Q57484322-3EDE9DB8-1CB7-41BE-8346-8835D165264A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-3EDE9DB8-1CB7-41BE-8346-8835D165264A
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P407
Q57484322-3EDE9DB8-1CB7-41BE-8346-8835D165264A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-3EDE9DB8-1CB7-41BE-8346-8835D165264A
rank
NormalRank
type
BestRank
Statement
P407
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