A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss
Abstract Background MYH14 gene mutations have been suggested to be associated with nonsyndromic/syndromic sensorineural hearing loss. It has been reported that mutations in MYH14 can result in autosomal dominant nonsyndromic deafness-4A (DFNA4). Methods In this study, we examined a four-generation H...
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| Автори: | , , , , , |
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| Формат: | Книга |
| Опубліковано: |
BMC,
2020-07-01T00:00:00Z.
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| Предмети: | |
| Онлайн доступ: | Connect to this object online. |
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Connect to this object online.3rd Floor Main Library
| Шифр: |
A1234.567 |
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| Примірник 1 | Доступно |