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Cavicchi C, Oussalah A, Falliano S, et al. PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations. Clin Epigenetics. 2021;13(1):137doi: 10.1186/s13148-021-01117-2.
Cavicchi, C., Oussalah, A., Falliano, S., Ferri, L., Gozzini, A., Gasperini, S., Motta, S., Rigoldi, M., Parenti, G., Tummolo, A., Meli, C., Menni, F., Furlan, F., Daniotti, M., Malvagia, S., la Marca, G., Chery, C., Morange, P. E., Tregouet, D., Donati, M. A., Guerrini, R., Guéant, J. L., & Morrone, A. (2021). PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations. Clinical epigenetics, 13(1), 137. https://doi.org/10.1186/s13148-021-01117-2
Cavicchi, Catia, et al. "PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations." Clinical epigenetics vol. 13,1 (2021): 137. doi: https://doi.org/10.1186/s13148-021-01117-2
Cavicchi C, Oussalah A, Falliano S, Ferri L, Gozzini A, Gasperini S, Motta S, Rigoldi M, Parenti G, Tummolo A, Meli C, Menni F, Furlan F, Daniotti M, Malvagia S, la Marca G, Chery C, Morange PE, Tregouet D, Donati MA, Guerrini R, Guéant JL, Morrone A. PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations. Clin Epigenetics. 2021 Jul 02;13(1):137. doi: 10.1186/s13148-021-01117-2. PMID: 34215320; PMCID: PMC8254308.
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