Should PMM2-deficiency (CDG Ia) be searched in every case of unexplained hydrops fetalis?
- 30 November 2010
- journal article
- case report
- Published by Elsevier BV in Molecular Genetics and Metabolism
- Vol. 101 (2-3), 253-257
- https://doi.org/10.1016/j.ymgme.2010.06.009
Abstract
No abstract availableKeywords
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