Ocular phenotype and therapeutic interventions in keratitis-ichthyosis-deafness (KID) syndrome.
Mc Lean K, Bignotti S, Callea M, Cammarata-Scalisi F, Steger B, Armstrong D, Lagan M, Sinton J, Semeraro F, Kaye SB, Romano V, Willoughby CE.
Mc Lean K, et al. Among authors: kaye sb.
Ophthalmic Genet. 2024 Feb;45(1):16-22. doi: 10.1080/13816810.2023.2258218. Epub 2024 Jan 26.
Ophthalmic Genet. 2024.
PMID: 37755702