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Q35568755-C5B4243C-37F1-4597-8FF5-2AF9282C49B0
Q35568755-C5B4243C-37F1-4597-8FF5-2AF9282C49B0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35568755-C5B4243C-37F1-4597-8FF5-2AF9282C49B0
Hyperekplexia (startle disease): a novel mutation (S270T) in the M2 domain of the GLRA1 gene and a molecular review of the disorder.
P2860
Q35568755-C5B4243C-37F1-4597-8FF5-2AF9282C49B0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35568755-C5B4243C-37F1-4597-8FF5-2AF9282C49B0
rank
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type
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wasDerivedFrom
a6e6f75d1e7f3bf03dbaf3049684950b4fa95324
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