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Guéant JL, Chéry C, Oussalah A, et al. Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nat Commun. 2018;9(1):554doi: 10.1038/s41467-018-03054-w.
Guéant, J. L., Chéry, C., Oussalah, A., Nadaf, J., Coelho, D., Josse, T., Flayac, J., Robert, A., Koscinski, I., Gastin, I., Filhine-Tresarrieu, P., Pupavac, M., Brebner, A., Watkins, D., Pastinen, T., Montpetit, A., Hariri, F., Tregouët, D., Raby, B. A., Chung, W. K., Morange, P. E., Froese, D. S., Baumgartner, M. R., Benoist, J. F., Ficicioglu, C., Marchand, V., Motorin, Y., Bonnemains, C., Feillet, F., Majewski, J., & Rosenblatt, D. S. (2018). Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nature communications, 9(1), 554. https://doi.org/10.1038/s41467-018-03054-w
Guéant, Jean-Louis, et al. "Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients." Nature communications vol. 9,1 (2018): 554. doi: https://doi.org/10.1038/s41467-018-03054-w
Guéant JL, Chéry C, Oussalah A, Nadaf J, Coelho D, Josse T, Flayac J, Robert A, Koscinski I, Gastin I, Filhine-Tresarrieu P, Pupavac M, Brebner A, Watkins D, Pastinen T, Montpetit A, Hariri F, Tregouët D, Raby BA, Chung WK, Morange PE, Froese DS, Baumgartner MR, Benoist JF, Ficicioglu C, Marchand V, Motorin Y, Bonnemains C, Feillet F, Majewski J, Rosenblatt DS. Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nat Commun. 2018 Feb 02;9(1):554. doi: 10.1038/s41467-018-03054-w. PMID: 29396438; PMCID: PMC5797229.
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