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Q28235848-EF84236A-E62F-4E30-B8FD-BE0FA2817AF7
Q28235848-EF84236A-E62F-4E30-B8FD-BE0FA2817AF7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-EF84236A-E62F-4E30-B8FD-BE0FA2817AF7
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor
P31
Q28235848-EF84236A-E62F-4E30-B8FD-BE0FA2817AF7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-EF84236A-E62F-4E30-B8FD-BE0FA2817AF7
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
469ac210a9bd89ef2e3c712e17fd2e431aca25d1
P31
scholarly article