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Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population

Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population

10.1186/s12952-015-0029-5

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書目詳細資料
Main Authors: Abu-Amero, K.K, Helwa, I, Al-Muammar, A, Strickland, S, Hauser, M.A, Allingham, R.R, Liu, Y
其他作者: DUKE-NUS MEDICAL SCHOOL
格式: Article
出版: 2020
主題:
adult
allele
Article
case control study
central corneal thickness
COL5A1 gene
controlled study
disease predisposition
female
FNDC3B gene
FOXO1 gene
gene
gene mutation
genetic analysis
genetic association
genetic susceptibility
genetic variability
genotype
human
keratoconus
LCN12 PTGDS gene
major clinical study
male
population research
promoter region
risk factor
RXRA COL5A1 gene
Saudi Arabia
single nucleotide polymorphism
cornea
genetic association study
genetic variation
genetics
health survey
pathology
procedures
young adult
Adult
Case-Control Studies
Cornea
Female
Genetic Association Studies
Genetic Variation
Humans
Keratoconus
Male
Population Surveillance
Young Adult
在線閱讀:https://scholarbank.nus.edu.sg/handle/10635/181447
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https://scholarbank.nus.edu.sg/handle/10635/181447

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