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Q30426940-561FD7D5-74AA-4FFE-8989-7DC853E35B11
Q30426940-561FD7D5-74AA-4FFE-8989-7DC853E35B11
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30426940-561FD7D5-74AA-4FFE-8989-7DC853E35B11
Glycine receptor mouse mutants: model systems for human hyperekplexia
P2860
Q30426940-561FD7D5-74AA-4FFE-8989-7DC853E35B11
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30426940-561FD7D5-74AA-4FFE-8989-7DC853E35B11
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wasDerivedFrom
0d31d57af334f0c5577bbc845ca1d07fd4671d97
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