Stevens, E. Et Al. 2013. Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of alpha-Dystroglycan. AMERICAN JOURNAL OF HUMAN GENETICS , vol.92, no.3 , 354-365.

Stevens, E., Carss, K. J., Cirak, S., Foley, R., Torelli, S., Willer, T., ... Tambunan, D. E.(2013). Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of alpha-Dystroglycan. AMERICAN JOURNAL OF HUMAN GENETICS , vol.92, no.3, 354-365.

Stevens, Elizabeth Et Al. "Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of alpha-Dystroglycan," AMERICAN JOURNAL OF HUMAN GENETICS , vol.92, no.3, 354-365, 2013

Stevens, Elizabeth Et Al. "Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of alpha-Dystroglycan." AMERICAN JOURNAL OF HUMAN GENETICS , vol.92, no.3, pp.354-365, 2013

Stevens, E. Et Al. (2013) . "Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of alpha-Dystroglycan." AMERICAN JOURNAL OF HUMAN GENETICS , vol.92, no.3, pp.354-365.

@article{article, author={Elizabeth Stevens Et Al. }, title={Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of alpha-Dystroglycan}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2013, pages={354-365} }