Certain common genetic changes might make some people with focal epilepsy less responsive to seizure medications, finds a new global study. Certain common genetic changes might make some people with ...
Investigators led by Northwestern Medicine scientists have identified mutations in a gene coding for a key ion channel in the brain as a new cause of a debilitating form of migraine, according to a ...
GWAS power plots. Power plots of current and future GWAS estimated using MiXeR (21), displaying the estimated proportion of SNP-heritability explained by genome-wide significant SNPs as a function of ...
The largest and most diverse study to date of epilepsy's genetic factors has revealed new potential targets for treatment, both shared by and unique to different subtypes of epilepsy. The findings ...
Certain common genetic changes might make some people with focal epilepsy less responsive to seizure medications, finds a new global study led by researchers at UCL and UTHealth Houston. Focal ...
STAMFORD, Conn.--(BUSINESS WIRE)-- GeneDx (Nasdaq: WGS), a leader in delivering improved health outcomes through genomic insights, today announced Biogen (Nasdaq: BIIB), Praxis Precision Medicines ...
uniQure QURE reported initial six-month follow-up results from the first low-dose cohort of six patients enrolled in its ongoing phase I/IIa study evaluating AMT-260, an investigational gene therapy ...
Hosted on MSN
Personalized gene therapy eased severe epilepsy in two boys, helping one walk independently
A 15-year-old boy with a severe genetic form of epilepsy walked on his own for the first time after receiving a custom-built antisense oligonucleotide designed to silence only the mutant copy of his ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results