Rapid detection of the hot spot gene mutations in Chinese patients with nonsyndromic hearing loss by polymerase chain reaction-restrictive fragment length polymorphism

Chinese Journal of Medical Genetics

Volumn 26, Issue 5, 2009, Pages 518-520

  Zhao, Juan ^a   Wu, Ling Qian ^a   Feng, Yong ^b   Hu, Hao ^a   Pan, Qian ^a   Xiong, Le Qin ^a   Liang, De Sheng ^a  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

12S rRNA gene; Deafness; GJB2 gene; Polymerase chain reaction restrictive fragment length polymorphism; SLC26A4 gene

Indexed keywords

CONNEXIN 26; RNA 12S;

ALLELE; ARTICLE; CHINESE; GENE; GENE MUTATION; HEARING LOSS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SLC26A4 GENE;

ADOLESCENT; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CONNEXINS; FEMALE; HEARING LOSS; HUMANS; MALE; MEMBRANE TRANSPORT PROTEINS; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; YOUNG ADULT;

EID: 70350726320     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: 10.3760/cma.j.issn.1003-9406.2009.05.008     Document Type: Article

References (7)

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