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...
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| Main Authors: | , , , , , , |
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| Format: | Book |
| Published: |
The Company of Biologists,
2016-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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