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The First Korean Case of MAN1B1-Congenital Disorder of Glycosylation Diagnosed Using Whole-exome Sequencing and Matrix-assisted Laser Desorption Ionization Time-of-flight Mass Spectrometry.
Kim KB, Lee GS, Shin S, Kim DC, Seo D, Kweon H, Kang H, Park S, Kim DH, Ryoo N, Lee S, Ha JS. Kim KB, et al. Among authors: park s. Ann Lab Med. 2024 Nov 7. doi: 10.3343/alm.2024.0226. Online ahead of print. Ann Lab Med. 2024. PMID: 39506209 Free article. No abstract available.
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