Modification of the PROM1 disease phenotype by a mutation in ABCA4.
Lee W, Paavo M, Zernant J, Stong N, Laurente Z, Bearelly S, Nagasaki T, Tsang SH, Goldstein DB, Allikmets R.
Lee W, et al. Among authors: paavo m.
Ophthalmic Genet. 2019 Aug;40(4):369-375. doi: 10.1080/13816810.2019.1660382. Epub 2019 Sep 6.
Ophthalmic Genet. 2019.
PMID: 31576780
Free PMC article.