Presents clinical, biochemical, and genetic information concerning those metabolic anomalies grouped under inborn errors of metabolism.DEFICIENCIES. Affected. Tissues. Erythrocytes are the cell type most likely to exhibit low or absent catalase activity. ... It has been shown that one Swiss-type variant enzyme can be electrophoretically separated from normal and that hybrid anbsp;...
|Title||:||The metabolic and molecular bases of inherited disease|
|Author||:||Charles R. Scriver|
|Publisher||:||McGraw-Hill Companies - 1995|