Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss. (Q50505554)
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scientific article published in January 1998
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss. |
scientific article published in January 1998 |
Statements
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss. (English)
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D A Scott
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M L Kraft
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R Carmi
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A Ramesh
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K Elbedour
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Y Yairi
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C R Srisailapathy
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S S Rosengren
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A F Markham
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R F Mueller
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N J Lench
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G Van Camp
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R J Smith
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V C Sheffield
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1 January 1998
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11
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5
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387-394
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