Ionis and Ultragenyx are competing to develop oligonucleotide treatments for Angelman syndrome, but will Neuren’s peptide ...

A disabled man is ‘powerless’ to oppose a ‘traumatising eviction’ from his care home of ten years due to a funding refusal ...

Angelman syndrome is caused by a large deletion of the region of the maternal chromosome that contains UBE3A, or by a DNA sequence change (mutation) in the UBE3A gene inherited from the mother.

We each get two copies of every gene - one copy from each of our parents. But what happens when one of these genes has been "turned off", or imprinted, and the remaining gene is defective?

Wednesday the young boy born with Angelman Syndrome made excellent progress on his walking skills while greeting those who ...

The date reflects the genetic defect Angelman Syndrome causes in the 15th chromosome and nods to Feburary’s designation as Rare Disease Month.

Ionis has committed to a phase 3 programme for its antisense therapy for rare genetic disorder Angelman syndrome, just weeks after Biogen decided against exercising an option to license the drug.

Laughing is one of the better-known traits of Angelman syndrome, a rare neurogenetic disorder that disrupts typical messaging in the brain. A single missing gene leads to the absence of a vital ...

an AI large model can generate alerts about potential rare genetic disorders, such as Rett syndrome or Angelman syndrome, or complex neurodevelopmental conditions within seconds, alongside medical ...

His family is in the beginning stages of fundraising for a service dog for Weston. The price tag for the dog is $10,000. Wednesday it was a packed house at Frankie's Bar in Hemlock and all eyes were ...