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Q34440826-9D31D156-0BD8-4795-A5A0-175854928FBA
Q34440826-9D31D156-0BD8-4795-A5A0-175854928FBA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34440826-9D31D156-0BD8-4795-A5A0-175854928FBA
High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p.
P2860
Q34440826-9D31D156-0BD8-4795-A5A0-175854928FBA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34440826-9D31D156-0BD8-4795-A5A0-175854928FBA
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wasDerivedFrom
e972763e9c35edf8c20789d01b4f4dd5a0c11c10
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