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Q28235848
Q28235848
Dataset
https://www.wikidata.org/wiki/Special:EntityData/Q28235848
Q28235848
Dataset
https://www.wikidata.org/wiki/Special:EntityData/Q28235848
about
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
dateModified
2019-10-27T20:00:50Z
http://www.w3.org/2001/XMLSchema#dateTime
version
1,039,921,991
http://www.w3.org/2001/XMLSchema#integer
identifiers
3
http://www.w3.org/2001/XMLSchema#integer
sitelinks
0
http://www.w3.org/2001/XMLSchema#integer
statements
15
http://www.w3.org/2001/XMLSchema#integer
type
Dataset