S-EPMC12903620 - Identification and functional characterization of a novel CRYBB1 deletion mutation causing autosomal dominant congenital cataract in a Chinese family. - OmicsDI

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

ABSTRACT:

SUBMITTER: Li L

PROVIDER: S-EPMC12903620 | biostudies-literature | 2026 Jan

REPOSITORIES: biostudies-literature