Should PMM2-deficiency (CDG Ia) be searched in every case of unexplained hydrops fetalis?
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Léticée N, et al. Among authors: ville y.
Mol Genet Metab. 2010 Oct-Nov;101(2-3):253-7. doi: 10.1016/j.ymgme.2010.06.009. Epub 2010 Jun 22.
Mol Genet Metab. 2010.
PMID: 20638314
Review.