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AJMG.A.37721
AJMG.A.37721
http://dx.doi.org/10.1002/AJMG.A.37721
A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy.
P356
Q52137131-DEEF47D4-7F1F-46BD-AF0D-6C05C8F23965
P356
AJMG.A.37721
http://dx.doi.org/10.1002/AJMG.A.37721