Some repeats of three or more nucleotides in tandem, which are present in a gene or in its vicinity, tend to increase in number and for this reason are called dynamic mutations. These triplet repeats are unstable and can expand from one generation to the next. According to the expansion size, an unaffected individual can carry a pre-mutation that will expand through generations leading to the development of triplet repeat expansion diseases. The increase in the number of repeats over time leads to earlier development and increased severity of symptoms in affected individuals in successive generations. Although there is still no treatment for this type of disease, several strategies are under investigation. Here, we describe treatmen...
Trinucleotide-repeat expansion diseases (TREDs) are a group of inherited human genetic disorders nor...
Trinucleotide-repeat expansion diseases (TREDs) are a group of inherited human genetic disorders nor...
The expansion of CAG•CTG trinucleotide repeat sequences has been identified as the genetic cause of ...
Some repeats of three or more nucleotides in tandem, which are present in a gene or in its vicinity...
Dynamic mutations involve expansion of the number of repeat units consisting of three or more nucle...
Dynamic mutations involve expansion of the number of repeat units consisting of three or more nucle...
The development of genetics in the last few decades is replete with surprise phenomena and new findi...
Background Inherited diseases caused by unstable repeated DNA sequences are rare, but together re...
Background Inherited diseases caused by unstable repeated DNA sequences are rare, but together re...
Background Inherited diseases caused by unstable repeated DNA sequences are rare, but together re...
Background Inherited diseases caused by unstable repeated DNA sequences are rare, but together re...
Background & Aims: Nearly 30 hereditary disorders in humans result from an increase in the number of...
Trinucleotide repeat disorders are an umbrella group of genetic diseases that have been well describ...
International audienceTrinucleotide repeat expansions are involved in more than two dozen neurologic...
Fourteen genetic neurodegenerative diseases and three fragile sites have been associated with the ex...
Trinucleotide-repeat expansion diseases (TREDs) are a group of inherited human genetic disorders nor...
Trinucleotide-repeat expansion diseases (TREDs) are a group of inherited human genetic disorders nor...
The expansion of CAG•CTG trinucleotide repeat sequences has been identified as the genetic cause of ...
Some repeats of three or more nucleotides in tandem, which are present in a gene or in its vicinity...
Dynamic mutations involve expansion of the number of repeat units consisting of three or more nucle...
Dynamic mutations involve expansion of the number of repeat units consisting of three or more nucle...
The development of genetics in the last few decades is replete with surprise phenomena and new findi...
Background Inherited diseases caused by unstable repeated DNA sequences are rare, but together re...
Background Inherited diseases caused by unstable repeated DNA sequences are rare, but together re...
Background Inherited diseases caused by unstable repeated DNA sequences are rare, but together re...
Background Inherited diseases caused by unstable repeated DNA sequences are rare, but together re...
Background & Aims: Nearly 30 hereditary disorders in humans result from an increase in the number of...
Trinucleotide repeat disorders are an umbrella group of genetic diseases that have been well describ...
International audienceTrinucleotide repeat expansions are involved in more than two dozen neurologic...
Fourteen genetic neurodegenerative diseases and three fragile sites have been associated with the ex...
Trinucleotide-repeat expansion diseases (TREDs) are a group of inherited human genetic disorders nor...
Trinucleotide-repeat expansion diseases (TREDs) are a group of inherited human genetic disorders nor...
The expansion of CAG•CTG trinucleotide repeat sequences has been identified as the genetic cause of ...