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Volumn 7, Issue 8, 2012, Pages

Prevalence and clinical features of hearing loss patients with cdh23 mutations: A large cohort study

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CDH23 GENE; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; GENE; GENE AMPLIFICATION; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; GENOTYPE; HEARING LOSS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MUTATIONAL ANALYSIS; PERCEPTION DEAFNESS; PHENOTYPE; PRESCHOOL CHILD; PREVALENCE; SCHOOL CHILD;

EID: 84865031797     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0040366     Document Type: Article
Times cited : (67)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.