A novel FBN1 mutation in a Chinese family with isolated ectopia lentis

Molecular Vision

Volumn 18, Issue , 2012, Pages 945-950

  Yang, Guoxing ^a   Chu, Meifang ^b   Zhai, Xinling ^c   Zhao, Jialiang ^a  

^a PEKING UNION MEDICAL COLLEGE HOSPITAL   (China)

^b Fourth Hospital of Xi'an City   (China)

^c Department of the Ophthalmology   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CYSTEINE; FIBRILLIN 1; GENOMIC DNA;

ADULT; AGED; ARTICLE; BLOOD SAMPLING; CHINESE; CLINICAL ARTICLE; CLINICAL STUDY; CODON; CONTROLLED STUDY; DNA EXTRACTION; ECTOPIA LENTIS; FAMILY HISTORY; FBN1 GENE; FEMALE; GENE; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; GENOTYPE; HUMAN; LEUKOCYTE; LINKAGE ANALYSIS; MICROSATELLITE MARKER; PRIORITY JOURNAL;

ADOLESCENT; ADULT; ANIMALS; ARGININE; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CASE-CONTROL STUDIES; CYSTEINE; ECTOPIA LENTIS; FEMALE; GENES, DOMINANT; HAPLOTYPES; HUMANS; LENS, CRYSTALLINE; MALE; MICROFILAMENT PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PHENOTYPE; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA;

EID: 84860859343     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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