Related references
Note: Only part of the references are listed.Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss
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Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome
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Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death
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A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome
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Human connexin disorders of the skin
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