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Q28235848-54B6C462-2540-4CA9-9B3F-0C4F2049C6ED
Q28235848-54B6C462-2540-4CA9-9B3F-0C4F2049C6ED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-54B6C462-2540-4CA9-9B3F-0C4F2049C6ED
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
P407
Q28235848-54B6C462-2540-4CA9-9B3F-0C4F2049C6ED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-54B6C462-2540-4CA9-9B3F-0C4F2049C6ED
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P407
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