-
involves the
elongation of
similar non-coding sequences,
specifically pentanucleotide repeats,
namely TTTCA and TTTTA,
within different genes. Myoclonus...
- in 2004, a
genetic basis was not
found till 2019, when a
biallelic pentanucleotide expansion in the RFC1 gene was
found to be a
cause of CANVAS. Symptoms...
- 50 to 150 base
pairs and
generally contain multiple copies of the
pentanucleotide AUUUA.
Early studies indicated that AREs can vary in
sequence and fall...
-
aphanidermatum and
Fusarium oxysporum f.sp. radicis-lycopersici. Di- to
pentanucleotide usage and the list of the most
abundant octa- to tetradecanucleotides...
- (ATXN10) 36
years 9
years ataxia,
seizures Mexico Chromosome 22q
linked pentanucleotide repeat SCA11 (TTBK2) 30 yrs (15–70)
Normal lifespan Mild,
remain ambulatory...
-
Repeat units of four and five
nucleotides are
referred to as tetra- and
pentanucleotide motifs, respectively. Most
eukaryotes have microsatellites, with the...
- CTG expansion.
Ataxin 10,
coded by ATXN10. It is ****ociated with the
pentanucleotide disorder, SCA10. Frataxin,
follows a
similar naming convention and...
- with the
downstream pentanucleotide microsatellite sequence. The
microsatellite is polymorphic, with a
varying number of
pentanucleotide repeats directly...
-
trinucleotide repeats,
expansions of one
tetranucleotide (CCTG), five
pentanucleotide (ATTCT, TGGAA, TTTTA, TTTCA, and AAGGG),
three hexanucleotide (GGCCTG...
- "[Spinocerebellar
ataxia type 10 (SCA10): a
disease caused by a
novel pentanucleotide repeat expansion]".
Rinsho Shinkeigaku. 41 (12): 1120–2. PMID 12235814...
