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GBB.12008
GBB.12008
http://dx.doi.org/10.1111/GBB.12008
Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes.
P356
Q43663646-E53286D6-A324-4E08-8255-2F82017CDD7D
P356
GBB.12008
http://dx.doi.org/10.1111/GBB.12008