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Q48117972-BF17E933-011E-4766-B20A-3076DDCC749A
Q48117972-BF17E933-011E-4766-B20A-3076DDCC749A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48117972-BF17E933-011E-4766-B20A-3076DDCC749A
KCNA2 mutations are rare in hereditary spastic paraplegia.
P2860
Q48117972-BF17E933-011E-4766-B20A-3076DDCC749A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48117972-BF17E933-011E-4766-B20A-3076DDCC749A
rank
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Statement
wasDerivedFrom
dc4294f8b912869b21427877ef92f0d634c49e20
P2860
A new Kv1.2 channelopathy underlying cerebellar ataxia.