Exclusion of lumican and fibromodulin as candidate genes in MYP3 linked high grade myopia

Molecular Vision

Volumn 10, Issue , 2004, Pages 917-922

  Paluru, Prasuna C ^a   Scavello, Genaro S ^a   Ganter, William R ^a   Young, Terri L ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN FIBRIL; FIBROMODULIN; LUMICAN; KERATAN SULFATE; PROTEOCHONDROITIN SULFATE; PROTEOGLYCAN; SCLEROPROTEIN;

3' UNTRANSLATED REGION; AMPLICON; ARTICLE; CHROMOSOME 12Q; CHROMOSOME 1Q; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; DNA SEQUENCE; EXON; GENE AMPLIFICATION; GENE EXPRESSION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC CODE; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; MYOPIA; PHENOTYPE; PRIORITY JOURNAL; REFRACTION ERROR; SEQUENCE ALIGNMENT; SINGLE NUCLEOTIDE POLYMORPHISM; CHILD; CHROMOSOME 1; CHROMOSOME 12; FEMALE; GENETIC LINKAGE; GENETICS; GENOTYPE; INFANT; MALE; NUCLEOTIDE SEQUENCE; PEDIGREE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD;

CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 12; DNA MUTATIONAL ANALYSIS; EXTRACELLULAR MATRIX PROTEINS; FEMALE; GENOTYPE; HUMANS; INFANT; KERATAN SULFATE; LINKAGE (GENETICS); LOD SCORE; MALE; MYOPIA; PEDIGREE; POLYMERASE CHAIN REACTION; PROTEOCHONDROITIN SULFATES; PROTEOGLYCANS; SEQUENCE ANALYSIS, DNA;

EID: 22044436256     PISSN: 10900535     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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