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CWY014
CWY014
http://dx.doi.org/10.1093/GLYCOB/CWY014
Variant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular features.
P356
Q49922672-BF64A37B-B978-4DB6-93D0-BB9D53565B88
P356
CWY014
http://dx.doi.org/10.1093/GLYCOB/CWY014