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Q26830661-9243F191-C304-490D-B52F-163815C47C34
Q26830661-9243F191-C304-490D-B52F-163815C47C34
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26830661-9243F191-C304-490D-B52F-163815C47C34
The impact of human hyperekplexia mutations on glycine receptor structure and function
P2860
Q26830661-9243F191-C304-490D-B52F-163815C47C34
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26830661-9243F191-C304-490D-B52F-163815C47C34
rank
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wasDerivedFrom
28ad215c7c947ab19845403a767192153f4fa136
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