Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mutation analysis of 12 genes in Chinese families with congenital cataracts.

Molecular vision - 1 Jan 2011

Sun Wenmin, Xiao Xueshan, Li Shiqiang, Guo Xiangming, Zhang Qingjiong

Abstract excerpt

PURPOSE: To identify mutations in 12 genes in Chinese families with congenital cataracts. METHODS: Twenty five families with congenital cataracts involved in this study. The coding exons and adjacent intronic regions of 12 genes were analyzed by cycle sequencing, including the alpha A crystallin (CRYAA), alpha B crystallin (CRYAB), beta A1 crystallin (CRYBA1), beta A4 crystallin (CRYBA4), beta B1 crystallin...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to alpha-Crystallin B Chain
Share to Asian People
Share to Cataract

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexins

Share to Crystallins

Share to gamma-Crystallins

Share to Heterozygote

Share to Sequence Alignment

Source

Open in PubMed Open full text

Identifiers

PMID: 21866213
PMCID: PMC3159683

Genes

CRYAA
GJA3
CRYAB
CRYBA1
CRYGD
CRYGS
CRYBA4
CRYBB1
CRYBB2
CRYBB3
CRYGC
GJA8

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation analysis of 12 genes in Chinese families with congenital cataracts.PMID 21866213Read ↗

Identification of mutations associated with congenital cataracts in nineteen Chinese familiesSemantic proximity Read ↗

Identification and characterization of six β-crystallin gene mutations associated with congenital cataract in Chinese families.Semantic proximity Read ↗

Four mutations identified in Chinese families with autosomal dominant congenital cataracts by next-generation sequencing.Semantic proximity Read ↗

Mutational spectrum in a Chinese cohort with congenital cataracts.Semantic proximity Read ↗

Mutation profiles of congenital cataract genes in 21 northern Chinese families.Semantic proximity Read ↗

Targeted Exome Sequencing of Congenital Cataracts Related Genes: Broadening the Mutation Spectrum and Genotype-Phenotype Correlations in 27 Chinese Han Families.Semantic proximity Read ↗

Novel mutations identified in Chinese families with autosomal dominant congenital cataracts by targeted next-generation sequencing.Semantic proximity Read ↗

Mutational screening of six genes in Chinese patients with congenital cataract and microcornea.Semantic proximity Read ↗

Identification of 4 Novel Variants in 19 Families with Congenital CataractsSemantic proximity Read ↗

[Analysis of disease-causing gene mutation in three Chinese families with congenital inherited cataract].Semantic proximity Read ↗

Mutation analysis of two families with inherited congenital cataracts.Semantic proximity Read ↗

Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.