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Q46383497-837F73A8-615C-4A9F-90F7-53E0465B25E0
Q46383497-837F73A8-615C-4A9F-90F7-53E0465B25E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46383497-837F73A8-615C-4A9F-90F7-53E0465B25E0
Hereditary hyperekplexia caused by novel mutations of GLRA1 in Turkish families.
P2860
Q46383497-837F73A8-615C-4A9F-90F7-53E0465B25E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46383497-837F73A8-615C-4A9F-90F7-53E0465B25E0
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wasDerivedFrom
56c8c407513239009c81b6b7ae39a7acc5b56db9
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