Trinucleotide repeats found ina) Huntigton's diseaseb) Spinocerebellar ataxiac) Amyotropic lateral sclerosisd) Sclerosis
High-Yield Explanation
Examples of trinucleotide repeat mutation :-
Huntignton's disease
Spinocerebella ataxia
Friedreich ataxia
Fragile - X-syndrome
Dystrophia myotanica
Dentorubral pallidoluysiane atrophy
X-chromosome spinobulbar muscular atrophy