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Volumn 36, Issue 3, 1999, Pages 260-261

Allele specific oligonucleotide analysis of the common deafness mutation 35delG in the connexin 26 (GJB2) gene

Author keywords

Connexin 26 gene; Deafness; Mutation 35delG

Indexed keywords

CONNEXIN 26; GUANINE; OLIGONUCLEOTIDE; THYMINE;

EID: 0033056952     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (24)

References (10)
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    • Li XC, Everett LA, Lalwani AK, et al. A mutation in PDS causes non-syndromic recessive deafness. Nat Genet 1998;18:215-17.
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  • 5
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    • Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
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    • Zelante L, Gasparini P, Estivill X, et al. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Hum Mol Genet 1997;6:1605-9.
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  • 7
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    • Denoyelle F, Weil D, Maw M, et al Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. Hum Mol Genet 1997;6:2173-7.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.