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Article

Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus.

BMJ open - 1 Apr 2016

Zhao Hui, Huang Xiu-Feng, Zheng Zhi-Li, Deng Wen-Li, Lei Xin-Lan, Xing Dong-Jun, Ye Liang, Xu Su-Zhong, Chen Jie, Zhang Fang, Yu Xin-Ping, Jin Zi-Bing

Abstract excerpt

OBJECTIVES: Infantile nystagmus (IN) is a genetically heterogeneous condition characterised by involuntary rhythmic oscillations of the eyes accompanied by different degrees of vision impairment. Two genes have been identified as mainly causing IN: FRMD7 and GPR143. The aim of our study was to identify the genetic basis of both sporadic IN and X-linked IN. DESIGN: Prospective analysis. PATIENTS: Twenty Chinese...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 27036142
DOI: 10.1136/bmjopen-2015-010649
PMCID: PMC4823450

Genes

FRMD7

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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