A rhesus macaque model of α‐dystroglycanopathy caused by a POMT1 splice altering variant
Abstract Background Biallelic mutations in genes associated with α‐dystroglycan glycosylation manifest in a spectrum of conditions referred to as α‐dystroglycanopathies, including Walker–Warburg syndrome, which primarily disrupt brain, eye, and muscle development. While small‐animal models for the disease have been dev...