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Article

Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation.

Ophthalmic genetics - 1 Sept 2013

McAnany J Jason, Alexander Kenneth R, Kumar Nalin M, Ying Hongyu, Anastasakis Anastasios, Fishman Gerald A

Abstract excerpt

PURPOSE: To document a novel NYX gene mutation in a patient with X-linked complete congenital stationary night blindness and to describe this patient's electroretinogram (ERG) characteristics. METHODS: ERGs were recorded from a 17-year-old male with a previously unreported NYX mutation (819G > A)...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 23289809
DOI: 10.3109/13816810.2012.743570
PMCID: PMC3842226

Genes

NYX
ERG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23289809-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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