Prevalence of GJB2 mutations in prelingual deafness in the Greek population

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Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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Connexin-26 mutations in sporadic and inherited sensorineural deafness

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Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

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Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

Leopoldo Zelante · Human Molecular Genetics · 1997 · 623 citations