Should PMM2-deficiency (CDG Ia) be searched in every case of unexplained hydrops fetalis?

Title
Should PMM2-deficiency (CDG Ia) be searched in every case of unexplained hydrops fetalis?
Authors
Keywords
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Journal
MOLECULAR GENETICS AND METABOLISM
Volume 101, Issue 2-3, Pages 253-257
Publisher
Elsevier BV
Online
2010-06-23
DOI
10.1016/j.ymgme.2010.06.009

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