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Article

Mutation screening of the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein congenital stationary night blindness.

Ophthalmic genetics - 1 Jan 2000

Dan Handong, Song Xiusheng, Li Jiazhang, Xing Yiqiao, Li Tuo

Abstract excerpt

BACKGROUND: Schubert-Bornschein congenital stationary night blindness (CSNB) is a rare retinal disorder that may lead to severe visual impairment in patients. The aim of this study was to detect mutations in the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein CSNB. MATERIALS AND METHODS: A cohort of eight unrelated Chinese probands with Schubert-Bornschein CSNB was recruited for this...

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Source

Identifiers

PMID: 27428514
DOI: 10.1080/13816810.2016.1193876

Genes

CABP4
GRM6
NYX
TRPM1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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