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

• Authors : Dan H; a Department of Ophthalmology , The Central Hospital of Enshi Autonomous Prefecture, Enshi Clinical College of Wuhan University , Enshi , China.; Song X

Subjects: Mutation*; Calcium-Binding Proteins/Calcium-Binding Proteins/Calcium-Binding Proteins/*genetics ; Eye Diseases, Hereditary/Eye Diseases, Hereditary/Eye Diseases, Hereditary/*genetics Night blindness, congenital stationary

• Source: Ophthalmic genetics [Ophthalmic Genet] 2017 May-Jun; Vol. 38 (3), pp. 206-210. Date of Electronic Publication: 2016 Jul 18.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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