| lysosomal storage disease |
An inherited disease characterized by a defect in the functional expression of any of the lysosomal enzymes.
출처: www.lsdn.com/glance_glossary.shtml
|
|---|---|
| lysosomal storage disease |
A disease caused by deficiency of specific lysosomal enzymes that normally degrade glycoproteins, glycolipids, or mucopolysaccharides. Thus, the substances that cannot be catabolized accumulate in lysosomes. Specific en
출처:
|
| lysosomal |
of or pertaining to a lysosome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| lysosomal α-glucosidase |
glucan 1,4-α-glucosidase.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| lysosomal α-glucosidase deficiency |
glycogen storage disease, type II.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|