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Article

Allelic variation of the FRMD7 gene in congenital idiopathic nystagmus.

Archives of ophthalmology (Chicago, Ill. : 1960) - 1 Sept 2007

Self James E, Shawkat Fatima, Malpas Crispin T, Thomas N Simon, Harris Christopher M, Hodgkins Peter R, Chen Xiaoli, Trump Dorothy, Lotery Andrew J

Abstract excerpt

OBJECTIVES: To perform a genotype-phenotype correlation study in an X-linked congenital idiopathic nystagmus pedigree (pedigree 1) and to assess the allelic variance of the FRMD7 gene in congenital idiopathic nystagmus. METHODS: Subjects from pedigree 1 underwent detailed clinical examination inc...

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Share to Cytoskeletal Proteins
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Diseases, X-Linked

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Share to Polymorphism, Single-Stranded Conformational

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Source

Identifiers

PMID: 17846367
DOI: 10.1001/archopht.125.9.1255

Genes

FRMD7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17846367-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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