It is carried on the X chromosome.
Sexlinked and recessive.
It is carried on the X chromosome.
Genes that are location on the sex chromosomes.
A corrected human hemophilia gene would be considered medicine, as it is aimed at treating a genetic disorder in humans.
It is a disorder which is passed on through your genes. It's actually quite simple. You see, hemophilia is hereditary, hence the "genetic". Then, it is a disorder of the blood, hence "disorder". "Genetic Disorder".
Hemophilia is one disease in which blood does not clot normally. von Willebrand's Disease
There is no chance that the child will have hemophilia even if the spouse has hemophilia. Any girls the couple has will be carriers if the spouse has hemophilia.
50%
Can anyone be a candidate for the hemophilia a
Hemophilia is caused by a deficiency of clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B).
50%
Because the gene that causes hemophilia is located on the X chromosome, so it will occur in males more frequently than in females.