Gene therapy via canalostomy approach preserves auditory and vestibular functions in a mouse model of Jervell and Lange-Nielsen syndrome type 2.
Nat Commun
; 12(1): 697, 2021 01 29.
Article
in En
| MEDLINE
| ID: mdl-33514733
Full text:
1
Database:
MEDLINE
Main subject:
Genetic Therapy
/
Semicircular Canals
/
Jervell-Lange Nielsen Syndrome
/
Potassium Channels, Voltage-Gated
/
Genetic Vectors
Type of study:
Prognostic_studies
Language:
En
Journal:
Nat Commun
Year:
2021
Type:
Article
Affiliation country:
China