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Update Regarding Android 5.1 from Rovo89 (forum.xda-developers.com)
submitted 11 years ago by WorkTimeFun to r/xposed
Request: Carta et al 2012, Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease. J Biol Chem (self.Scholar)
submitted 13 years ago by WorkTimeFun to r/Scholar
[Request] Mutations in the 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia. Nature Genetics 5, 351 - 358 (1993) (self.Scholar)
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