What are the genotypes of people who get huntington' s disease

Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disease with the typical manifestations of involuntary movements, psychiatric and behavior disorders, and cognitive impairment. It is caused by the dynamic mutation in CAG triplet repeat number in exon 1 of huntingtin (HTT) gene.

When a virus infects a host cell, it uses the cell's machinery to make copies of its own genetic material in a process called replication. finally, during the process of self-assembly, that protein shell and the copies of the virus's genetic material are assembled into new viruses.