<span>The right answer is D. males have only one copy of the X chromosome.
</span>Hemophilia is a rare hereditary bleeding disorder disease. The blood of hemophiliacs does not coagulate normally. Bleeding is not more important, but without treatment, they can be more frequent and last longer than normal. Hence the importance of good monitoring and good treatment.
<span>The 2 types of hemophilia A and B are recessive and X-linked, but a third of hemophilia correspond to a de novo mutation. It is observed that a man who wears the X is always affected by the disease (because he has only one X chromosome in its genome) whereas the woman is only a carrier (she has two X chromosomes, so it can carry a safe X and a mutated X without being attempted by the disease but can transmit it to her descendants). This must be taken into account for genetic counseling.</span>
In eukaryotic cells the DNA is in the nucleus.
but in prokaryotic cells, it's in the
cytoplasm
good luck
Answer:
Voltage-gated Ca2+ channels
Explanation:
Modulation of Ca+2 channel Epinephrine also causes an increase in cAMP that stimulates PKA that is protein kinase A, which in turn phosphorylates the voltage-gated Ca+2 channel that is the L channel. This phosphorylation results in a protein conformational change that enchances the channels activity.
