Synaptic roles for phosphomannomutase type 2 in a new Drosophila congenital disorder of glycosylation disease model

• المؤلفون الرئيسيون: William M. Parkinson (مؤلف), Michelle Dookwah (مؤلف), Mary Lynn Dear (مؤلف), Cheryl L. Gatto (مؤلف), Kazuhiro Aoki (مؤلف), Michael Tiemeyer (مؤلف), Kendal Broadie (مؤلف)
• التنسيق: كتاب
• منشور في: The Company of Biologists, 2016-05-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Congenital disorders of glycosylation (CDGs) constitute a rapidly growing family of human diseases resulting from heritable mutations in genes driving the production and modification of glycoproteins. The resulting symptomatic hypoglycosylation causes multisystemic defects that include severe neurol...