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Q28257487-7D9B4056-2396-43B3-8535-CD2F3034C92A
Q28257487-7D9B4056-2396-43B3-8535-CD2F3034C92A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28257487-7D9B4056-2396-43B3-8535-CD2F3034C92A
Recessive hyperekplexia mutations of the glycine receptor alpha1 subunit affect cell surface integration and stability
P2860
Q28257487-7D9B4056-2396-43B3-8535-CD2F3034C92A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28257487-7D9B4056-2396-43B3-8535-CD2F3034C92A
rank
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Statement
wasDerivedFrom
d87c6315744ca7c480c12f4b433253e49868a9ae
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