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S10048-013-0371-Z
S10048-013-0371-Z
http://dx.doi.org/10.1007/S10048-013-0371-Z
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3.
P356
Q47705355-93AD748E-D8C1-44A5-A42E-242F3B46B707
P356
S10048-013-0371-Z
http://dx.doi.org/10.1007/S10048-013-0371-Z