Huntington's Disease Prognosis
Huntington’s disease is caused by a mutation that occurs in the Huntingtin (HTT) gene, which is located on chromosome 4. The mutation exists as an expansion mutation of the trinucelotide cytosine-adenine-guanine (CAG). The length of this CAG expansion determines the severity and onset of the disease. Generally, the number of CAG repeats accounts for 60% of the variation in how […]
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