High frequency of GJB2 gene mutations in polish patients with prelingual nonsyndromic deafness

Genetic Testing

Volumn 5, Issue 2, 2001, Pages 147-148

  Wiszniewski, W ^a   Sobieszczanska Radoszewska, L ^a   Nowakowska Szyrwinska, E ^a   Obersztyn, E ^a   Bal, J ^a  

^a INSTITUTE OF MOTHER AND CHILD   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

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

ARTICLE; CHILD; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC EPIDEMIOLOGY; HEARING IMPAIRMENT; HEREDITY; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; POLAND; POPULATION RESEARCH;

EID: 0034863872     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/109065701753145637     Document Type: Article

References (5)

1. Prelingual deafness: High prevalence of a 30delG mutation in the connexin 26 gene
2. High carrier frequency of the 35delG deafness mutation in European populations
3. Connexin-26 mutations in hereditary non-syndromic sensorineural deafness
4. Genes responsible for human hereditary deafness: Symphony of thousand
5. Allele specific oligonucleotide analysis (ASO) for the common mutation 35delG in the connexin26 (GJB2) gene