GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects

Acta Oto-Laryngologica

Volumn 128, Issue 3, 2008, Pages 297-303

  Guo, Yu Fen ^a   Liu, Xiao Wen ^a   Guan, Jing ^a,c   Han, Ming Kun ^b   Wang, Da Yong ^b   Zhao, Ya Li ^c   Rao, Shao Qi ^b,d   Wang, Qiu Ju ^b  

^a LANZHOU UNIVERSITY   (China)

^b CHINESE PLA GENERAL HOSPITAL   (China)

^c INSTITUTE OF BASIC MEDICAL SCIENCES   (China)

^d HARBIN MEDICAL UNIVERSITY   (China)

Author keywords

Chinese; Genetic testing; Non syndromic hearing loss; Prelingual deafness

Indexed keywords

MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; DNA ISOLATION; ENZYME DEGRADATION; ETHNICITY; FEMALE; FRAMESHIFT MUTATION; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC VARIABILITY; GJB2 GENE; HEARING; HEARING IMPAIRMENT; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SLC26A4 GENE;

ADOLESCENT; ADULT; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CHINA; DEAFNESS; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; EXONS; FEMALE; GENE FREQUENCY; GENETIC SCREENING; GENETICS, POPULATION; HETEROZYGOTE DETECTION; HOMOZYGOTE; HUMANS; MALE; REFERENCE VALUES; SEQUENCE ANALYSIS, DNA;

EID: 39349099735     PISSN: 00016489     EISSN: 16512553     Source Type: Journal    
DOI: 10.1080/00016480701767382     Document Type: Article

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