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Q24676418-29AEEB44-9709-4718-99BE-07A2296F02CE
Q24676418-29AEEB44-9709-4718-99BE-07A2296F02CE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676418-29AEEB44-9709-4718-99BE-07A2296F02CE
A novel mutation (Gln266-->His) in the alpha 1 subunit of the inhibitory glycine-receptor gene (GLRA1) in hereditary hyperekplexia
P2860
Q24676418-29AEEB44-9709-4718-99BE-07A2296F02CE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676418-29AEEB44-9709-4718-99BE-07A2296F02CE
rank
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Statement
wasDerivedFrom
c2cf510b837e3b28321779dfe62ed31c95403946
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