Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT. (Q50493860)
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scientific article published in November 2000
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT. |
scientific article published in November 2000 |
Statements
Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT. (English)
1 reference
I Lerer
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M Sagi
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E Malamud
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H Levi
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A Raas-Rothschild
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D Abeliovich
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1 November 2000
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95
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1
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53-56
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