Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract

Molecular Vision

Volumn 19, Issue , 2013, Pages 835-844

  Bennett, Thomas M ^a   Maraini, Giovanni ^b   Jin, Chongfei ^c   Sun, Wenmin ^c   Fielding Hejtmancik, J ^c   Shiels, Alan ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF PARMA   (Italy)

^c NATIONAL EYE INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

ADOLESCENT; ADULT; AMPLICON; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE CONTROL STUDY; CHROMOSOME 19Q; COHORT ANALYSIS; EUROPEAN AMERICAN; FAMILY; FERRITIN BLOOD LEVEL; FTL GENE; GENE; GENE EXPRESSION PROFILING; GENE MAPPING; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HAPLOTYPE; HEREDIATRY HYPERFERRITINEMIA CATARACT SYNDROME; HETEROZYGOSITY; HUMAN; HYPERFERRITINEMIA; IN SITU HYBRIDIZATION; IRON RESPONSIVE ELEMENT; LEUKOCYTE; LINKAGE ANALYSIS; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SENILE CATARACT; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ADULT; AGING; ANIMALS; APOFERRITINS; BASE SEQUENCE; CATARACT; CHILD; CHILD, PRESCHOOL; DNA, INTERGENIC; FEMALE; GENES, DOMINANT; GENETIC LINKAGE; HUMANS; INFANT; IRON; LENS, CRYSTALLINE; LOD SCORE; MALE; MICE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; RESPONSE ELEMENTS; YOUNG ADULT;

EID: 84876223601     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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