Novel frizzled-4 gene mutations in Chinese patients with familial exudative vitreoretinopathy

Archives of Ophthalmology

Volumn 128, Issue 10, 2010, Pages 1341-1349

  Jia, Li Yun ^a   Li, Xiao Xin ^a   Yu, Wen Zhen ^a   Zeng, Wo Tan ^b   Liang, Chen ^b  

^a PEKING UNIVERSITY PEOPLE S HOSPITAL   (China)

^b CHINESE NATIONAL HUMAN GENOME CENTER AT SHANGHAI   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHINESE; CLINICAL ARTICLE; CONTROLLED STUDY; ETHNICITY; EXON; EYE EXAMINATION; EYE REFRACTION; FAMILIAL EXUDATIVE VITREORETINOPATHY; FEMALE; FRAMESHIFT MUTATION; FRIZZLED 4 GENE; GENE DELETION; GENE MUTATION; GENE SEQUENCE; GENETIC CONSERVATION; GENETIC SCREENING; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HUMAN; HUMAN GENOME; INFANT; MALE; MISSENSE MUTATION; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY; VISUAL ACUITY; VITREORETINOPATHY; AMINO ACID SEQUENCE; ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; EPIDEMIOLOGY; EXUDATE; EYE DISEASE; GENETICS; GENOTYPE; MOLECULAR GENETICS; MUTATION; PEDIGREE; PHENOTYPE; PRESCHOOL CHILD; RETINA DISEASE; VITREOUS BODY; YOUNG ADULT;

FRIZZLED PROTEIN; FZD4 PROTEIN, HUMAN; G PROTEIN COUPLED RECEPTOR;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CHINA; DNA MUTATIONAL ANALYSIS; EXUDATES AND TRANSUDATES; EYE DISEASES; FEMALE; FRIZZLED RECEPTORS; GENOTYPE; HUMANS; INFANT; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; RECEPTORS, G-PROTEIN-COUPLED; RETINAL DISEASES; VITREOUS BODY; YOUNG ADULT;

EID: 77958004304     PISSN: 00039950     EISSN: 15383601     Source Type: Journal    
DOI: 10.1001/archophthalmol.2010.240     Document Type: Article

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