Meta-analysis of GJB2 mutation 35delG frequencies in Europe

Genetic Testing

Volumn 5, Issue 2, 2001, Pages 149-152

  Lucotte, G ^a   Mercier, G ^a  

^a Center of Molecular Neurogenetics   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; GENE PRODUCT; GJB2 PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; EUROPE; FRANCE; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC EPIDEMIOLOGY; GENETIC SCREENING; GEOGRAPHIC DISTRIBUTION; HEARING IMPAIRMENT; HUMAN; META ANALYSIS; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; RANDOMIZED CONTROLLED TRIAL;

EID: 0034876240     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/109065701753145646     Document Type: Article

References (10)

1. High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness
2. Prelingual deafness: High prevalence of a 30delG mutation in the connexin 26 gene
3. Connexin-26 mutations in sporadic and inherited sensorineural deafness
4. High carrier frequency of the 35delG deafness mutation in European populations. Genetic analysis consortium of GJB2 35delG
5. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
6. Northwest/south-east gradient of ΔF508 frequency in Europe
7. PCR test for diagnosis of the common GJB2-35delG mutation on dried blood spots
8. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness
9. Determination for the carrier frequency of the common GJB2 connexin-26 35deIG mutation in the Belgian population using an easy reliable screening method
10. Connexin 26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans