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Synaptic roles for phosphomannomutase type 2 in a new Drosophila congenital disorder of glycosylation disease model
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...
में बचाया:
| में प्रकाशित: | Dis Model Mech |
|---|---|
| मुख्य लेखकों: | , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
The Company of Biologists Ltd
2016
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4892659/ https://ncbi.nlm.nih.gov/pubmed/26940433 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.022939 |
| टैग : |
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