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Q30179423-7FA69801-2392-41CF-9F88-C6A7BDB9595E
Q30179423-7FA69801-2392-41CF-9F88-C6A7BDB9595E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30179423-7FA69801-2392-41CF-9F88-C6A7BDB9595E
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.
P2860
Q30179423-7FA69801-2392-41CF-9F88-C6A7BDB9595E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30179423-7FA69801-2392-41CF-9F88-C6A7BDB9595E
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Statement
wasDerivedFrom
7bd98cf65aa63495b8cb708c459f0ce78f64bf09
P2860
Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1