Mutations of the POMT1 gene found in patients with Walker–Warburg syndrome lead to a defect of protein O-mannosylation
- 3 December 2004
- journal article
- Published by Elsevier BV in Biochemical and Biophysical Research Communications
- Vol. 325 (1), 75-79
- https://doi.org/10.1016/j.bbrc.2004.10.001
Abstract
No abstract availableKeywords
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