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Q28119046-3128C7CE-D5E0-4B4C-AFEA-A690BAB92E71
Q28119046-3128C7CE-D5E0-4B4C-AFEA-A690BAB92E71
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Statement
http://www.wikidata.org/entity/statement/Q28119046-3128C7CE-D5E0-4B4C-AFEA-A690BAB92E71
The human glycine receptor subunit alpha3. Glra3 gene structure, chromosomal localization, and functional characterization of alternative transcripts
P2860
Q28119046-3128C7CE-D5E0-4B4C-AFEA-A690BAB92E71
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28119046-3128C7CE-D5E0-4B4C-AFEA-A690BAB92E71
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wasDerivedFrom
1ebe0dcbdbfe0ae5aef057796ddcfc1b9185d8e2
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