Answer: <em>D. Causes an accumulation of lipids in brain cells</em>
Explanation:
Tay-Sachs disease is caused by a genetic mutation in the <em>HEXA</em> gene. It is an autosomal recessive disease that causes the mutation on an enzyme, which metabolizes <em>GM2 Ganglioside</em> in nerve cells, this leads to a build-up of the molecule in brain cells. At the moment there is no cure for the disease, only support treatment is available.
Answer:
changes in temperature that happen with increasing altitude.
The expected result of this poison on secondary active transport is that the poison will prevents the conformational changes which are necessary for the pump to perform its function, thus preventing it from been able to carry out transportation of ions in and out of the cell.
