Low-frequency coding variants in CETP and CFB are associated with susceptibility of exudative age-related macular degeneration in the Japanese population

Human Molecular Genetics

Volumn 25, Issue 22, 2016, Pages 5027-5034

  Momozawa, Yukihide ^a   Akiyama, Masato ^a,b   Kamatani, Yoichiro ^a   Arakawa, Satoshi ^b,c   Yasuda, Miho ^b   Yoshida, Shigeo ^b   Oshima, Yuji ^b   Mori, Ryusaburo ^d   Tanaka, Koji ^d   Mori, Keisuke ^e,f   Inoue, Satoshi ^e   Terasaki, Hiroko ^g   Yasuma, Tetsuhiro ^g   Honda, Shigeru ^h   Miki, Akiko ^h   Inoue, Maiko ⁱ   Fujisawa, Kimihiko ^c   Takahashi, Kanji ^j   Yasukawa, Tsutomu ^k   Yanagi, Yasuo ^l,m,n   Kadonosono, Kazuaki ^o   Sonoda, Koh Hei ^b   Ishibashi, Tatsuro ^b   Takahashi, Atsushi ^a   Kubo, Michiaki ^a   more..

^a Institute of Physical and Chemical Research   (Japan)

^b KYUSHU UNIVERSITY   (Japan)

^c KYUSHU HOSPITAL   (Japan)

^d SURUGADAI NIHON UNIVERSITY HOSPITAL   (Japan)

^e SAITAMA MEDICAL UNIVERSITY   (Japan)

^f International University of Health and Welfare   (Japan)

^g NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^h KOBE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

ⁱ YOKOHAMA CITY UNIVERSITY MEDICAL CENTER   (Japan)

^j KANSAI MEDICAL UNIVERSITY   (Japan)

^k NAGOYA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICAL SCIENCES   (Japan)

^l UNIVERSITY OF TOKYO   (Japan)

^m SINGAPORE EYE RESEARCH INSTITUTE   (Singapore)

ⁿ SINGAPORE NATIONAL EYE CENTRE   (Singapore)

^o YOKOHAMA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

more..

Author keywords

[No Author keywords available]

Indexed keywords

AGE RELATED MACULAR DEGENERATION; ARTICLE; BLINDNESS; C2 GENE; CETP GENE; CFB GENE; CONTROLLED STUDY; DISEASE PREDISPOSITION; ETHNICITY; GENE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOME-WIDE ASSOCIATION STUDY; HAPLOTYPE; HUMAN; JAPANESE (PEOPLE); MAJOR CLINICAL STUDY; MULTIPLEX POLYMERASE CHAIN REACTION; POLYPOIDAL CHOROIDAL VASCULOPATHY; PRIORITY JOURNAL; RETINA DISEASE; RETINAL ANGIOMATOUS PROLIFERATION; SINGLE NUCLEOTIDE POLYMORPHISM; AGED; CASE CONTROL STUDY; FEMALE; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; JAPAN; MACULAR DEGENERATION; MALE; METABOLISM; NUCLEOTIDE SEQUENCE; PROCEDURES;

ALTERNATIVE COMPLEMENT PATHWAY C3 C5 CONVERTASE; CETP PROTEIN, HUMAN; CHOLESTEROL ESTER TRANSFER PROTEIN; COMPLEMENT COMPONENT C2; COMPLEMENT FACTOR H;

AGED; BASE SEQUENCE; CASE-CONTROL STUDIES; CHOLESTEROL ESTER TRANSFER PROTEINS; COMPLEMENT C2; COMPLEMENT FACTOR B; COMPLEMENT FACTOR H; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HAPLOTYPES; HUMANS; JAPAN; MACULAR DEGENERATION; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 85015795343     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddw335     Document Type: Article

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