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Q42691767-76AFF413-7057-4DB1-8D9D-41E226955A78
Q42691767-76AFF413-7057-4DB1-8D9D-41E226955A78
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Statement
http://www.wikidata.org/entity/statement/Q42691767-76AFF413-7057-4DB1-8D9D-41E226955A78
Massive sequencing of 70 genes reveals a myriad of missing genes or mechanisms to be uncovered in hereditary spastic paraplegias.
P2860
Q42691767-76AFF413-7057-4DB1-8D9D-41E226955A78
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42691767-76AFF413-7057-4DB1-8D9D-41E226955A78
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wasDerivedFrom
3207a0d73c13686f0780261c43829e72fd776212
P2860
A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18)