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Q44125053-F165DBB3-A5A3-461D-92BA-C4D78F06ECBC
Q44125053-F165DBB3-A5A3-461D-92BA-C4D78F06ECBC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44125053-F165DBB3-A5A3-461D-92BA-C4D78F06ECBC
Major and minor form of hereditary hyperekplexia.
P2860
Q44125053-F165DBB3-A5A3-461D-92BA-C4D78F06ECBC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44125053-F165DBB3-A5A3-461D-92BA-C4D78F06ECBC
rank
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type
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Statement
wasDerivedFrom
a7b5297b335ff51e54a9077201bcb4032736d8d5
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