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Q47629156-FDA31CFD-7FCF-42D9-B277-38C6CF68B5BC
Q47629156-FDA31CFD-7FCF-42D9-B277-38C6CF68B5BC
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http://www.wikidata.org/entity/statement/Q47629156-FDA31CFD-7FCF-42D9-B277-38C6CF68B5BC
Ethnicity can predict GLRA1 genotypes in hyperekplexia.
P2860
Q47629156-FDA31CFD-7FCF-42D9-B277-38C6CF68B5BC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47629156-FDA31CFD-7FCF-42D9-B277-38C6CF68B5BC
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wasDerivedFrom
93dd9ecc6653375f32d4249b04a1892254d06429
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