Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility

Investigative Ophthalmology and Visual Science

Volumn 52, Issue 3, 2011, Pages 1748-1754

  Spencer, Kylee L ^a   Olson, Lana M ^a   Schnetz Boutaud, Nathalie ^a   Gallins, Paul ^b   Wang, Gaofeng ^b   Scott, William K ^b   Agarwal, Anita ^c   Jakobsdottir, Johanna ^d   Conley, Yvette ^e   Weeks, Daniel E ^e   Gorin, Michael B ^f   Pericak Vance, Margaret A ^b   Haines, Jonathan L ^a  

^a VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^b UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^c VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^d UNIVERSITY OF CHICAGO   (United States)

^e UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

^f UCLA MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AGED; ARTICLE; CACNG3 GENE; CAUCASIAN; CHROMOSOME 16P; CONTROLLED STUDY; FAMILY STUDY; FEMALE; GENE; GENE EXPRESSION PROFILING; GENE FUNCTION; GENE IDENTIFICATION; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HS3ST4 GENE; HUMAN; IL4R GENE; ITGAM GENE; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; MOLECULAR PATHOLOGY; PRIORITY JOURNAL; Q7Z6F8 GENE; RETINA MACULA AGE RELATED DEGENERATION; SINGLE NUCLEOTIDE POLYMORPHISM;

AGED; CALCIUM CHANNELS; CHROMOSOMES, HUMAN, PAIR 16; FEMALE; GENE EXPRESSION REGULATION; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; LINKAGE DISEQUILIBRIUM; LOD SCORE; MACULAR DEGENERATION; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS;

EID: 79955958047     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.09-5112     Document Type: Article

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