Identification and functional characterization of a novel CRYBB1 deletion mutation causing autosomal dominant congenital cataract in a Chinese family

Ophthalmology AND mitochondrial

BMC Ophthalmol. 2026 Jan 20. doi: 10.1186/s12886-026-04624-z. Online ahead of print.

NO ABSTRACT

PMID:41559635 | DOI:10.1186/s12886-026-04624-z