Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss
β Scribed by M Wagatsuma; R Kitoh; H Suzuki; H Fukuoka; Y Takumi; S Usami
- Book ID
- 110888427
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 165 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0009-9163
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Mutations in the GJB2 gene encoding the gap-junction protein connexin 26 have been identified in many patients with childhood hearing impairment (HI). One single mutation, c.35delG, accounts for the majority of mutations in Caucasian patients with HI. In the present study we screened 500 healthy con
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