Use of adenine base editing and homology-independent targeted integration strategies to correct the cystic fibrosis causing variant, W1282X

  1. Mention, K.
  2. Cavusoglu-Doran, K.
  3. Joynt, A.T.
  4. Santos, L.
  5. Sanz, D.
  6. Eastman, A.C.
  7. Merlo, C.
  8. Langfelder-Schwind, E.
  9. Scallan, M.F.
  10. Farinha, C.M.
  11. Cutting, G.R.
  12. Sharma, N.
  13. Harrison, P.T.
Revista:
Human molecular genetics

ISSN: 1460-2083

Ano de publicación: 2023

Volume: 32

Número: 23

Páxinas: 3237-3248

Tipo: Artigo

DOI: 10.1093/HMG/DDAD143 GOOGLE SCHOLAR lock_openAcceso aberto editor
Fonte de datos: Scopus