Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients

  1. Zeuli, R.
  2. Karali, M.
  3. de Bruijn, S.E.
  4. Rodenburg, K.
  5. Scarpato, M.
  6. Capasso, D.
  7. Astuti, G.D.N.
  8. Gilissen, C.
  9. Rodríguez-Hidalgo, M.
  10. Ruiz-Ederra, J.
  11. Testa, F.
  12. Simonelli, F.
  13. Cremers, F.P.M.
  14. Banfi, S.
  15. Roosing, S.
Aldizkaria:
Human Genetics and Genomics Advances

ISSN: 2666-2477

Argitalpen urtea: 2024

Alea: 5

Zenbakia: 3

Mota: Artikulua

DOI: 10.1016/J.XHGG.2024.100314 GOOGLE SCHOLAR lock_openSarbide irekia editor
Datuen iturria: Scopus