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Q35549382-ED28ADBB-EEB3-4EB5-A535-8ABFB20C79E5
Q35549382-ED28ADBB-EEB3-4EB5-A535-8ABFB20C79E5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35549382-ED28ADBB-EEB3-4EB5-A535-8ABFB20C79E5
A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18)
P31
Q35549382-ED28ADBB-EEB3-4EB5-A535-8ABFB20C79E5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35549382-ED28ADBB-EEB3-4EB5-A535-8ABFB20C79E5
rank
NormalRank
type
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Statement
wasDerivedFrom
c8cb7ed26515c71f9c2a16a00e8633f4c26a34d5
P31
scholarly article