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PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations

Overview of attention for article published in Clinical Epigenetics, July 2021
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7 Dimensions

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10 Mendeley
Summary X Dimensions citations
So far, Dimensions has found 7 publications that cite this research output.

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