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Paper Details

APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.
Nat Commun
53
2018
APRDX1 mutant allele, CCDC163P, H3K36me3, MMACHC, MMACHC locus, PRDX1, blood, cblC, epi-cblC, epiallele, fibroblasts, gene trios, germlines, inborn errors of vitamin B12 metabolism, man, patients, sperm, vitamin B12
Author NameAffiliation
Tomi PastinenMcGill University and Research Institute McGill University Health Centre
Alexandre MontpetitMcGill University and Research Institute McGill University Health Centre
Alexandre MontpetitMcGill University and Research Institute McGill University Health Centre
Benjamin A RabyBrigham and Women's Hospital, Harvard Medical School
Wendy K ChungColumbia University
Wendy K ChungColumbia University
Jean-Fran??ois Benoist
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