Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss (Q33855117)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss |
scientific article |
Statements
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Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss (English)
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E S Cohn
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P M Kelley
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1 September 1999
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89
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130-136
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Identifiers
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