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S10038-017-0408-5
S10038-017-0408-5
http://dx.doi.org/10.1038/S10038-017-0408-5
Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutations.
P356
Q48102552-FF155E5A-317E-464E-98DC-CC2F5391916F
P356
S10038-017-0408-5
http://dx.doi.org/10.1038/S10038-017-0408-5