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Q48106459-5D216A1D-D55C-40ED-AE90-D1FBA9C1E848
Q48106459-5D216A1D-D55C-40ED-AE90-D1FBA9C1E848
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48106459-5D216A1D-D55C-40ED-AE90-D1FBA9C1E848
Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type.
P2860
Q48106459-5D216A1D-D55C-40ED-AE90-D1FBA9C1E848
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48106459-5D216A1D-D55C-40ED-AE90-D1FBA9C1E848
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Statement
wasDerivedFrom
21ca2296156993949c798a92297357e53488f2ee
P2860
Arthrogryposis as a Syndrome: Gene Ontology Analysis