Fingerprint
Dive into the research topics of 'Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan
Elizabeth Stevens, Keren J. Carss, Sebahattin Cirak, A. Reghan Foley, Silvia Torelli, Tobias Willer, Dimira E. Tambunan, Shu Yau, Lina Brodd, Caroline A. Sewry, Lucy Feng, Goknur Haliloglu, Diclehan Orhan, William B. Dobyns, Gregory M. Enns, Melanie Manning, Amanda Krause, Mustafa A. Salih, Christopher A. Walsh, Matthew Hurles
Research output: Contribution to journal › Article › peer-review
151
Scopus
citations