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Article

Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts.

Molecular vision - 4 Mar 2008

Li Feifeng, Wang Shuzhen, Gao Chang, Liu Shiguo, Zhao Baojian, Zhang Meng, Huang Shangzhi, Zhu Siquan, Ma Xu

Abstract excerpt

PURPOSE: We sought to identify the genetic defect in a four-generation Chinese family with autosomal dominant congenital coralliform cataracts and demonstrate the functional analysis of a candidate gene in the family. METHODS: Family history data were recorded. Clinical and ophthalmologic examinations were performed on affected and unaffected family members. All the members were genotyped with microsatellite...

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Source

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Identifiers

PMID: 18334953
PMCID: PMC2268897

Genes

CRYGD

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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