The pathogenesis of common Gjb2 mutations associated with human hereditary deafness in mice
Cited by 2
Related Papers
Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivo
|Nature Biotechnology|2014|1.5k
AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial
|The Lancet|2024|323
AAV‐Mediated Gene Therapy Restores Hearing in Patients with DFNB9 Deafness
|Advanced Science|2024|176
BMAL1 knockout macaque monkeys display reduced sleep and psychiatric disorders
|National Science Review|2019|164