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Q53323741-416956FA-D60F-416A-8A93-4B4A18EB0A64
Q53323741-416956FA-D60F-416A-8A93-4B4A18EB0A64
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53323741-416956FA-D60F-416A-8A93-4B4A18EB0A64
A founder mutation p.H701P identified as a major cause of SPG7 in Norway.
P2860
Q53323741-416956FA-D60F-416A-8A93-4B4A18EB0A64
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53323741-416956FA-D60F-416A-8A93-4B4A18EB0A64
rank
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type
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Statement
wasDerivedFrom
5a94bfe21796042aecc31f5fa0a063925bb78d39
P2860
Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.