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Mutation Screening of Six Exons of ABCA4 in Iranian Stargardt Disease Patients.

Ensieh DarbariHamid AhmadiehNarsis DaftarianMozhgan Rezaei KanaviFatemeh SuriHamideh SabbaghiElahe Elahi
Published in: Journal of ophthalmic & vision research (2022)
mutations are heterogeneous among Iranian patients, and p.Gly1961Glu may be relatively frequent.
Keyphrases
  • newly diagnosed
  • patient reported