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Q34195421-A2BE5C83-7BAF-4622-B081-893EFC8CFBC5
Q34195421-A2BE5C83-7BAF-4622-B081-893EFC8CFBC5
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http://www.wikidata.org/entity/statement/Q34195421-A2BE5C83-7BAF-4622-B081-893EFC8CFBC5
Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P₂ phosphatase FIG4.
P2860
Q34195421-A2BE5C83-7BAF-4622-B081-893EFC8CFBC5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34195421-A2BE5C83-7BAF-4622-B081-893EFC8CFBC5
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type
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wasDerivedFrom
5d48f7d2b2477e62255fba9b175685d6087cf31c
P2860
Mutation of FIG4 causes a rapidly progressive, asymmetric neuronal degeneration.