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MAN1B1 deficiency: an unexpected CDG-II.
PLoS Genet. 2013;9(12):e1003989. doi: 10.1371/journal.pgen.1003989. Epub 2013 Dec 12.
PLoS Genet. 2013.
PMID: 24348268
Free PMC article.
Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDG.
Matthijs G, Rymen D, Millón MB, Souche E, Race V.
Matthijs G, et al. Among authors: millon mb.
Glycoconj J. 2013 Jan;30(1):67-76. doi: 10.1007/s10719-012-9445-7. Epub 2012 Sep 15.
Glycoconj J. 2013.
PMID: 22983704
Review.
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Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation?
Millón MB, Delgado MA, Azar NB, Guelbert N, Sturiale L, Garozzo D, Matthijs G, Jaeken J, de Kremer RD, Asteggiano CG.
Millón MB, et al.
JIMD Rep. 2011;1:65-72. doi: 10.1007/8904_2011_18. Epub 2011 Jun 22.
JIMD Rep. 2011.
PMID: 23430830
Free PMC article.
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