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Q28139306-A2047B0F-D661-4CC2-9C03-6CC5DB07031B
Q28139306-A2047B0F-D661-4CC2-9C03-6CC5DB07031B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28139306-A2047B0F-D661-4CC2-9C03-6CC5DB07031B
Hyperekplexia in the first year of life
P2860
Q28139306-A2047B0F-D661-4CC2-9C03-6CC5DB07031B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28139306-A2047B0F-D661-4CC2-9C03-6CC5DB07031B
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wasDerivedFrom
a908533661db1cb99f1e07ac5dd147904ba40be2
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