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S41525-017-0009-4
S41525-017-0009-4
http://dx.doi.org/10.1038/S41525-017-0009-4
Familial STAG2 germline mutation defines a new human cohesinopathy.
P356
Q47165215-2982A73E-5855-47AA-A751-939FF80EACF3
P356
S41525-017-0009-4
http://dx.doi.org/10.1038/S41525-017-0009-4