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Article

FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus.

Molecular vision - 3 Aug 2007

Zhang Qingjiong, Xiao Xueshan, Li Shiqiang, Guo Xiangming

Abstract excerpt

PURPOSE: To identify mutations causing X-linked congenital motor nystagmus (XL-CMN) in Chinese families. METHODS: Genomic DNA was prepared from peripheral blood leukocytes. Cycle sequencing was used to detect the sequence variation of the FERM domain containing 7 (FRMD7) gene, where mutations have been identified recently to associate with XL-CMN. RESULTS: Sequencing of the coding and the adjacent intron regions...

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Source

Identifiers

PMID: 17768376

Genes

FRMD7

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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