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s10048-013-0371-z
s10048-013-0371-z
https://scigraph.springernature.com/pub.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.
P2888
Q47705355-224F5C06-BF9A-45B7-8607-FB017AA452AE
P2888
s10048-013-0371-z
https://scigraph.springernature.com/pub.10.1007/s10048-013-0371-z