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Q28346777-C742D245-492C-460C-AD13-9BBB57046E08
Q28346777-C742D245-492C-460C-AD13-9BBB57046E08
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28346777-C742D245-492C-460C-AD13-9BBB57046E08
Hyperekplexia in neonates
P2860
Q28346777-C742D245-492C-460C-AD13-9BBB57046E08
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28346777-C742D245-492C-460C-AD13-9BBB57046E08
rank
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wasDerivedFrom
0e08842f1624eed39c2f4dd782b988a3d355f620
P2860
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