Associated Papers
Crystal structures of β-1,4-N-acetylglucosaminyltransferase 2: structural basis for inherited muscular dystrophies.
Yang JY et al.
Acta Crystallographica. Section D, Structural Biology, 2021
Milder forms of muscular dystrophy associated with POMGNT2 mutations.
Endo Y et al.
Neurology. Genetics, 2015
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome.
Manzini MC et al.
American Journal of Human Genetics, 2012
Select a paper to view details