Stevens et al., 2013 - Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of alpha-Dystroglycan. American journal of human genetics   92(3):354-365 Full text @ Am. J. Hum. Genet.
Morpholino List (4 Records)
Target Reagent
b3galnt2 MO1-b3galnt2
MO2-b3galnt2
dag1 MO1-dag1
tp53 MO4-tp53
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