Associated Papers
Prime editing optimized RTT permits the correction of the c.8713C>T mutation in DMD gene.
Happi Mbakam C et al.
Molecular Therapy. Nucleic Acids, 2022
Rare KCNJ18 variants do not explain hypokalaemic periodic paralysis in 263 unrelated patients.
Kuhn M et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2016
The sex-specific associations of the aromatase gene with Alzheimer's disease and its interaction with IL10 in the Epistasis Project.
Medway C et al.
European Journal of Human Genetics : Ejhg, 2014
Select a paper to view details