trinucleotide repeat expansion การใช้

• Both FXS and FXTAS are caused by a trinucleotide repeat expansion in FMR1.
• Many human diseases have been reported to be associated with trinucleotide repeat expansions including Huntington's disease.
• A CTG trinucleotide repeat expansion that is incorporated into the SCA8 but not the KLHL1 transcript causes spinocerebellar ataxia type 8.
• The key sequence which is found in Huntington's disease is a trinucleotide repeat expansion of glutamine residues beginning at the 18th amino acid.
• "' Trinucleotide repeat disorders "'( also known as "'trinucleotide repeat expansion disorders "', "'triplet repeat expansion disorders "'or "'codon reiteration disorders "') are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation where genomic sequences.
• "' Trinucleotide repeat disorders "'( also known as "'trinucleotide repeat expansion disorders "', "'triplet repeat expansion disorders "'or "'codon reiteration disorders "') are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation where genomic sequences.