PTC124 targets nonsense mutations
Research Highlights
Serious diseases genes revealed
A major advance in understanding the genetics behind several of the world’s most common diseases has been reported. The landmark Wellcome Trust study analysed DNA from the blood of 17,000 people to find genetic differences. They found new genetic variants for depression, Crohn’s disease, coronary heart disease, hypertension, rheumatoid arthritis and type 1 and 2… Continue reading Serious diseases genes revealed
Human genome further unravelled
A close-up view of the human genome
Gene deletions as frequent as mutations
In the most common form of HSP
SPG3A mutations important cause of HSP
SPG3A more often associated with a neuropathy
Gene SPG11 and HSP
Associated with cognitive defects
Genetic screening tests sometimes unreliable
Scientists find family members with HSP symptoms sometimes test falsely negative
REEP – a new HSP gene discovered
The third-most common HSP-causing gene
Support for spastin mutation screening
Bulgarian research first to show course of HSP related to type of mutation
SP Foundation (USA) makes research grant awards
The SP Foundation (USA) awards half a million dollars in research grants
