Recurrent mutations in the deafness geneGJB2 (connexin 26) in British Asian families

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 GeneOriginal Research · 1997 · 638 citations
2. 2Connexin-26 mutations in sporadic and inherited sensorineural deafnessOriginal Research · 1998 · 647 citations
3. 3Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossOriginal Research · 1998 · 252 citations
4. 4Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansOriginal Research · 1997 · 632 citations
5. 5Prevalent connexin 26 gene (GJB2) mutations in JapaneseOriginal Research · 2000 · 388 citations