학술논문
PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations
Document Type
Article
Author
Cavicchi, C.; Falliano, S.; Ferri, L.; Gozzini, A.; Guerrini, R.; Morrone, A.; Oussalah, A.; Chery, C.; Guéant, J.-L.; Gasperini, S.; Motta, S.; Rigoldi, M.; Parenti, G.; Tummolo, A.; Meli, C.; Menni, F.; Furlan, F.; Daniotti, M.; Donati, M.A.; Malvagia, S.; la Marca, G.; Morange, P.-E.; Tregouet, D.
Source
In: Clinical Epigenetics . (Clinical Epigenetics, December 2021, 13(1))
Subject
Language
English
ISSN
18687083
18687075
18687075