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302716
302716
http://dx.doi.org/10.1086/302716
Predominance of the T14484C mutation in French-Canadian families with Leber hereditary optic neuropathy is due to a founder effect.
P356
Q42698605-D4B76F5F-FDDC-44D0-8A50-F6D2FBB1D13B
P356
302716
http://dx.doi.org/10.1086/302716