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Q44095428-9D8A577A-CD55-4F76-8F56-4B01FD5A68FB
Q44095428-9D8A577A-CD55-4F76-8F56-4B01FD5A68FB
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http://www.wikidata.org/entity/statement/Q44095428-9D8A577A-CD55-4F76-8F56-4B01FD5A68FB
Functional characterization of compound heterozygosity for GlyRalpha1 mutations in the startle disease hyperekplexia.
P2860
Q44095428-9D8A577A-CD55-4F76-8F56-4B01FD5A68FB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44095428-9D8A577A-CD55-4F76-8F56-4B01FD5A68FB
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wasDerivedFrom
57f90a6db3c9af232f8d76b5edbde2299ddd9503
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