A mutation in CRX causing pigmented paravenous retinochoroidal atrophy. Oh JK, Nuzbrokh Y, Lee W, Lima de Carvalho JR Jr, et al. Eur J Ophthalmol 2022;32:NP235-NP239.

Read + Share

Amedeo Smart

Independent Medical Education

Read + Share

Oh JK, Nuzbrokh Y, Lee W, Lima de Carvalho JR Jr, et al. A mutation in CRX causing pigmented paravenous retinochoroidal atrophy. Eur J Ophthalmol 2022;32:NP235-NP239.
PMID: 32927963