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Q28592620-F2B4B21F-AFFC-45C5-BFE2-97BDA739DB24
Q28592620-F2B4B21F-AFFC-45C5-BFE2-97BDA739DB24
BestRank
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http://www.wikidata.org/entity/statement/Q28592620-F2B4B21F-AFFC-45C5-BFE2-97BDA739DB24
Transient neuromotor phenotype in transgenic spastic mice expressing low levels of glycine receptor beta-subunit: an animal model of startle disease.
P2860
Q28592620-F2B4B21F-AFFC-45C5-BFE2-97BDA739DB24
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28592620-F2B4B21F-AFFC-45C5-BFE2-97BDA739DB24
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type
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Statement
wasDerivedFrom
cfc5a53d58838b190aadff6edbf453e2faf224f8
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