A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families (Q33864995)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families |
scientific article |
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A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families (English)
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E Maestrini
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B P Korge
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J Ocaña-Sierra
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E Calzolari
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S Cambiaghi
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P M Scudder
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C S Munro
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Identifiers
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