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MGG3.72
MGG3.72
http://dx.doi.org/10.1002/MGG3.72
A-TWinnipeg: Pathogenesis of rare ATM missense mutation c.6200C>A with decreased protein expression and downstream signaling, early-onset dystonia, cancer, and life-threatening radiotoxicity
P356
Q33960818-23A29BED-FDBA-4028-9614-6E1F5A1A29A6
P356
MGG3.72
http://dx.doi.org/10.1002/MGG3.72