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S11655-014-1813-7
S11655-014-1813-7
http://dx.doi.org/10.1007/S11655-014-1813-7
Role of heteroplasmic mutations in the mitochondrial genome and the ID4 gene promoter methylation region in the pathogenesis of chronic aplastic anemia in patients suffering from Kidney yin deficiency.
P356
Q41004047-C746994B-863B-47FA-8807-43DD81B5BA1E
P356
S11655-014-1813-7
http://dx.doi.org/10.1007/S11655-014-1813-7