Mutation analysis of the Cx26, Cx30, and Cx31 genes in autosomal recessive nonsyndromic hearing impairment

Acta Oto-Laryngologica

Volumn 128, Issue 10, 2008, Pages 1056-1062

  Gürtler, Nicolas ^a,b,d   Egenter, Carole ^c   Bösch, Nemya ^c   Plasilova, Martina ^c  

^a Hals Nasen Ohrenklinik   (Switzerland)

^b HNO Universitatsklinik   (Switzerland)

^c UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

^d HNO Klinik   (Switzerland)

Author keywords

Autosomal recessive; Cochlear implant; Connexin; MLPA; Nonsyndromic hearing impairment

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE NONSYNDROMIC HEARING IMPAIRMENT; CONNEXIN 26 GENE; CONNEXIN 30 GENE; CONNEXIN 31 GENE; CONTROLLED STUDY; GENE; GENE AMPLIFICATION; GENE DELETION; GENE DUPLICATION; GENE IDENTIFICATION; GENE MUTATION; GENE PROBE; GENE SEQUENCE; HEARING IMPAIRMENT; HUMAN; INNER EAR DISEASE; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; POINT MUTATION; PREVALENCE; PRIORITY JOURNAL;

CASE-CONTROL STUDIES; COCHLEAR IMPLANTS; COHORT STUDIES; CONNEXINS; DEAFNESS; DNA MUTATIONAL ANALYSIS; GENE DELETION; GENE FREQUENCY; GENOTYPE; HUMANS; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; SENSITIVITY AND SPECIFICITY;

EID: 51649092548     PISSN: 00016489     EISSN: 16512553     Source Type: Journal    
DOI: 10.1080/00016480701854727     Document Type: Article

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