deletion
recessive
Huntington's disease is caused by a gene mutation, specifically in the HTT gene on chromosome 4.
No, it's caused by a single point mutation of a gene.
cystic fibrosis
sickle-cell anemia.
Huntington's disease is an example of a lethal dominant mutation. It is a neurodegenerative disorder caused by a dominant mutation in the HTT gene, leading to progressive loss of motor and cognitive functions, eventually resulting in death.
For example, some diseases caused by insertional mutations include: Fragile X Syndrome. Huntington's Disease. Myotonic dystrophy. Cystic fibrosis.
There are many thousands of different mutations.
A mutation is a permanent change in the DNA sequence of a gene. It may be a minor or a major change; and may be harmful or beneficial.RegardsTime is imaginary
Cystic fibrosis is primarily caused by mutations in the CFTR gene, which is located on chromosome 7. These mutations can result in a defective or non-functioning CFTR protein, leading to the characteristic symptoms of the disease.
Monogenetic disorders are caused by a mutation in a single gene. The mutation may be present on one or both chromosomes (one chromosome inherited from each parent). Examples of monogenic disorders are: sickle cell disease, cystic fibrosis, polycystic kidney disease, and Tay-Sachs disease.
No, HIV is a communicable disease caused by a virus, not by genetics.