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Q24517906-199B68C2-C6CE-4239-80AF-02C53543A45E
Q24517906-199B68C2-C6CE-4239-80AF-02C53543A45E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24517906-199B68C2-C6CE-4239-80AF-02C53543A45E
Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis
P2860
Q24517906-199B68C2-C6CE-4239-80AF-02C53543A45E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24517906-199B68C2-C6CE-4239-80AF-02C53543A45E
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wasDerivedFrom
8892388d68b7cc3dcb325154cb54ffff3abc19b8
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