- brancher enzyme
- branching enzyme 1,4-α-glucan branching enzyme.
Medical dictionary. 2011.
brancher enzyme
Look at other dictionaries:
brancher enzyme — branch·er en·zyme (branchґər enґzīm) 1,4 α glucan branching enzyme … Medical dictionary
brancher enzyme deficiency — branch·er en·zyme de·fi·cien·cy (branchґər enґzīm) glycogen storage disease, type IV … Medical dictionary
14-α-glucan branching enzyme — 1,4 α glu·can branch·ing en·zyme (glooґkan branchґing enґzīm) [EC 2.4.1.18] an enzyme of the transferase class that catalyzes the cleavage of internal α 1,4 glucoside linkages in glycogen (or, in plants, amylopectin) and transfer… … Medical dictionary
Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… … Medical dictionary
Glycogen storage disorders — ▪ Table Glycogen storage disorders (GSDs) type enzyme defect clinical features type I (von Gierke disease) glucose 6 phosphatase hypoglycemia, enlarged liver and kidneys, gastrointestinal symptoms, nosebleeds, short stature, gout type II (Pompe… … Universalium
glycogenosis — Any of the glycogen deposition diseases characterized by accumulation of glycogen of normal or abnormal chemical structure in tissue; there may be enlargement of the liver, heart, or striated muscle, including the … Medical dictionary
deficiency — An insufficient quantity of some substance (as in dietary d. or hemoglobin d. in marrow aplasia); organization (as in mental d.); activity (as in enzyme d. or reduced oxygen carrying capacity of the blood), etc., of which the amount present is of … Medical dictionary
type IV — an autosomal recessive disorder due to mutation in the GBE1 gene (locus: 3p12), which encodes the glycogen branching enzyme (1,4 α glucan branching enzyme), resulting in accumulation of long insoluble glycogen molecules with unbranched outer … Medical dictionary
