Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss (Q28139583)
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scientific article (publication date: 2000)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss |
scientific article (publication date: 2000) |
Statements
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss (English)
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1 January 2000
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9
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1
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63-7
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