Contribution of 1425G/A polymorphism in protein kinase C-Eta (PRKCH) gene and brain white matter lesions to the risk of sudden sensorineural hearing loss in a Japanese nested case-control study

Journal of Neurogenetics

Volumn 25, Issue 3, 2011, Pages 82-87

  Uchida, Yasue ^a,b   Sugiura, Saiko ^a   Nakashima, Tsutomu ^c   Ando, Fujiko ^a,d   Shimokata, Hiroshi ^a  

^a NATIONAL CENTER FOR GERIATRICS AND GERONTOLOGY   (Japan)

^b AICHI MEDICAL UNIVERSITY   (Japan)

^c NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d AICHI SHUKUTOKU UNIVERSITY   (Japan)

Author keywords

Brain MRI; Polymorphism; Protein kinase C eta; Sudden sensorineural hearing loss; White matter lesions

Indexed keywords

PROTEIN KINASE C ETA;

ADULT; ALLELE; ARTICLE; BRAIN DAMAGE; CASE CONTROL STUDY; CLINICAL ASSESSMENT; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENETIC HETEROGENEITY; GENETIC POLYMORPHISM; HUMAN; HUMAN CELL; HYPOTHESIS; JAPAN; MAJOR CLINICAL STUDY; MALE; MULTIVARIATE LOGISTIC REGRESSION ANALYSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOGENESIS; PERCEPTION DEAFNESS; PREVALENCE; PRIORITY JOURNAL; STROKE; WHITE MATTER;

ADULT; AGED; BRAIN; CASE-CONTROL STUDIES; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HEARING LOSS, SUDDEN; HUMANS; JAPAN; LONGITUDINAL STUDIES; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; NERVE FIBERS, MYELINATED; ODDS RATIO; POLYMORPHISM, GENETIC; PROTEIN KINASE C; RISK FACTORS;

EID: 80052768731     PISSN: 01677063     EISSN: 15635260     Source Type: Journal    
DOI: 10.3109/01677063.2011.591462     Document Type: Article

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