Mutations can result from spontaneous events or external mutagens.
A change in DNA sequence may change the pattern of protein folding, resulting in genetic disease.
Some genetic diseases may be caused by the substitution of only one incorrect amino acid in a protein.
It is possible for the substitution of one base for another to have no effect on an organism.
this disease leads to persistent brain malfunctioning
The more risk factors for a disease, the greater the chance of developing that disease.
All options are correct.
Sickle-cell disease
cancer
The molecular cause of Pick disease are a series of mutations linked to chromosomes 17, 9 and 3
CMT is caused by mutations in genes that produce proteins involved in the structure and function of either the peripheral nerve axon or the myelin sheath. Although different proteins are abnormal in different forms of CMT disease, all of the mutations affect the normal function of the peripheral nerves. The gene mutations in CMT disease are usually inherited.
A person with Canavan disease has changes (mutations) in both of the genes responsible for producing the enzyme aspartoacylase
disease is the correct spelling disease is the correct spelling
Genetic mutations passed from parent to child cause hereditary disease.
Mutations in two independent genes result in the clinical features of this disease.
No. It arises due to point mutations (like A -> T).