The perfect match for a face is not always the case.
When I was a child, I always thought my eyes would always be red.
That was not true.
The natural color of my skin has changed over the years.
My eyes now have a red tint.
I can’t even tell you how many times I have thought about looking into the mirror to see what my eyes look like, and I was always disappointed because I could not tell that I was red.
I have always wondered why.
When I started researching the causes of my red eyes, I came across a study that showed that my mother’s eye color was caused by her parents’ eye color.
I found the study to be a bit of a surprise.
The study found that a gene that causes eye color in females was in a couple of different gene families.
The researchers found that some of the genes that cause eye color have a genetic component that makes them less active when a gene is mutated.
That means that when a mutation occurs, the gene that was in the gene family that had the gene mutation is not active.
That way, the person who inherited the mutation would not be affected by it.
The researchers found a gene family in a few different gene family(s).
They named that gene family DYS388(DYS388) for its unique function.
They were also able to look at the effects of the mutations on eye color and found that if one mutation affects the DYS389 gene, the mutation affects all of the other genes in that gene’s family.
In the case of the Dys389 gene family, one of the changes that affected eye color is that the DY388 gene mutation also affects a gene called DYS390.
That gene is very active, so when the mutation occurs in that particular gene, that gene is inactivated.
The reason that it is not inactivated is because it is a member of a family of genes called DYP19, or Double-stranded DNA.
These genes have many functions, and when they are mutated, the changes make them less functional.
The result is that when the mutations occur, the other members of that gene are not activated.
The other members are more active, and they can take over some of what the other member of that family does.
The other important reason that a mutation affects an eye color gene is because of an enzyme called keratin.
When keratin is damaged, it can lead to problems with the skin and the eyes.
In a study published in the Journal of Investigative Dermatology, researchers looked at how the enzyme keratin changes in people with normal eye color, as well as people with red or irises.
The keratin that was damaged is called keratinsin.
When a person with normal color has a mutation that affects this enzyme, the affected eye changes.
When that happens, the eye changes color.
That changes how a person looks.
It’s a very good indicator of the condition of the eye.
The team found that people who had red eyes had significantly higher levels of the enzyme in their eye compared to the people who did not have red eyes.
The level of keratin in their eyes was about 1.5 times higher in the people with increased keratin levels compared to those with normal-eye color.
People with the mutation had much higher levels in their keratin compared to normal-eyed people.
This is because the mutations in this enzyme affect the function of the protein keratin, and it is also a factor that affects the activity of the gene, DY389, which is involved in the process of making collagen and keratin for the eyes, and also in the production of the pigment called melanin, the white pigment that gives skin its color.
So the mutation that caused my red eye could be the result of the keratin damage, or it could be something else that caused the eye to change.
If you have a mutation, you have higher keratin levels in your eye.
And if you have the mutation, your keratin could be more active.
You could also be more sensitive to the effects that your mutation is having on the enzyme, which could make you more sensitive.
If this mutation causes you to have red irises, it could also cause the eyes to turn a bit red.
You might see redness and lightening of the skin around the eyes or a very reddish-pinkish glow.
That is called erythema pigmentosum, or epidermal hyperpigmentation.
People who have this mutation also have a higher risk of developing skin cancers.
The person who has the mutation can have more keratin on their skin, which can make it more difficult for the skin to absorb moisture, and this could lead to a dry skin and an increased risk of skin cancer.
The skin that has more keratinoin in it can absorb moisture better, which allows it to grow more quickly.