Metabolism — Flashcards

What is the mode of inheritance of glycogen storage diseases?_____

_____ is a plasma transport protein for T3/T4.

Mild deficiencies of vitamin B3 cause _____

Can a urine test for ketones detect acetoacetate?_____

Which lysosomal storage disease may be treated with recombinant enzyme therapy? _____

In 21-hydroxylase deficiency, there is an increased level of urinary _____

S-adenosylmethionine (SAM) is a _____ donor

What is the initial breakdown product of epinephrine?_____

Nicotinamides (NAD+, NADP+) come from Vitamin _____

What part of the cell is the site of steroid synthesis and detoxification of drugs and poisons?_____