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CCR3.834
CCR3.834
http://dx.doi.org/10.1002/CCR3.834
FMR1 premutation with Prader-Willi phenotype and fragile X-associated tremor/ataxia syndrome.
P356
Q33625894-D9B94A2D-292F-4286-8DD6-68F0F694B77A
P356
CCR3.834
http://dx.doi.org/10.1002/CCR3.834