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316896
316896
http://dx.doi.org/10.1086/316896
A novel homoplasmic mutation in mtDNA with a single evolutionary origin as a risk factor for cardiomyopathy
P356
Q34144436-3B6ECA3F-9031-4348-B35D-170992B49DDE
P356
316896
http://dx.doi.org/10.1086/316896