The N1 gene mutation causes a rare disorder that could be responsible for a number of different neurological and psychiatric disorders. It has been linked in particular to schizophrenia, which can be treated with medication.
There are a number of things that can be done to minimize the risk of developing these diseases in the first place. For example, most of the people who have the N1 gene mutation have not been exposed to the environmental toxins that seem to be causing the genetic mutations.
A mutation of that kind is more likely to occur in children, especially if the parents are also genetically susceptible to the same disease. It also only seems to occur in males, so if you have a male parent who is also genetically susceptible to the disease, you may be at increased risk to develop it yourself. The chances of you having the N1 mutation are about 1 in 3 million.
I think the N1 mutation is a bit of a stretch since it’s only a mutation, and not one that needs to be exposed to chemicals. It’s not like this mutation was caused by a person with a disease; the gene mutation is caused by a person who has had a stressful life event.
The reason I brought this up is because while there is definitely a genetic predisposition for the N1 mutation, it is not as common in males as females. And more importantly, it’s not a “man thing” like breast cancer and birth defects. There are a handful of genes that are thought to be responsible for certain forms of cancer, and in fact one of the rarest forms of cancer does not actually involve a particular gene.
The fact is that, while the gene mutation is known to be more common in males, the fact is that, with the exception of a very few rare instances, that the N1 mutation does not affect male fertility. In fact, there has been a suggestion that it could increase male fertility.
The N1 gene mutation, however, is known to predispose to cancer. The point is that the N1 gene mutation has been found to be more common in males, more than half of all cases of non-familial breast cancer and half of all cases of non-familial non-familial cancer have the mutation.
This is not a surprise to me. The N1 mutation is found in 70% of males and 70% of females.
The N1 mutation is more common in males, and the male-specificity is due to the fact that the gene is located on the X chromosome. This is what makes the mutation more prevalent in males. It is also why the mutation is found in only half of all males. The female-specificity is due to the fact that the gene is located on the Y chromosome. This is what makes the mutation less prevalent in females.
This mutation causes a rare condition known as the N1, which is a rare disease with no known known cure. In the case of the N1 mutation, it results in a person’s brain being blocked by a substance called N1N-A. In other words, the brain is unable to receive and transmit information. The brain isn’t able to process information in the way that the rest of the body can. The information that can flow into the brain is severely limited.