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Q24338670-65E0D712-A3D0-49AF-AAB7-0D494C147667
Q24338670-65E0D712-A3D0-49AF-AAB7-0D494C147667
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http://www.wikidata.org/entity/statement/Q24338670-65E0D712-A3D0-49AF-AAB7-0D494C147667
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.
P2860
Q24338670-65E0D712-A3D0-49AF-AAB7-0D494C147667
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24338670-65E0D712-A3D0-49AF-AAB7-0D494C147667
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wasDerivedFrom
7eab541f42a593d0f5c717b53952af895762c2b6
P2860
Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia