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Q35549382-7768C560-58AE-420F-8816-189F9A9A04F0
Q35549382-7768C560-58AE-420F-8816-189F9A9A04F0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35549382-7768C560-58AE-420F-8816-189F9A9A04F0
A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18)
P2860
Q35549382-7768C560-58AE-420F-8816-189F9A9A04F0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35549382-7768C560-58AE-420F-8816-189F9A9A04F0
rank
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type
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Statement
wasDerivedFrom
253291b3da7817387e4fb26b7ef33785ecdf5dcd
P2860
A frameshift mutation of ERLIN2 in recessive intellectual disability, motor dysfunction and multiple joint contractures