Case of cone dystrophy with normal fundus appearance associated with biallelic POC1B variants.
Kominami A, Ueno S, Kominami T, Nakanishi A, Ito Y, Fujinami K, Tsunoda K, Hayashi T, Kikuchi S, Kameya S, Iwata T, Terasaki H.
Kominami A, et al. Among authors: nakanishi a.
Ophthalmic Genet. 2018 Apr;39(2):255-262. doi: 10.1080/13816810.2017.1408846. Epub 2017 Dec 8.
Ophthalmic Genet. 2018.
PMID: 29220607